Recalls in February 2025

OdorStop has issued a recall for about 13,000 boot and shoe dryers and deodorizers because the heat or ozone on-off switch can short circuit, resulting in arcing, and posing a fire hazard. No incidents have been reported.

The product was sold online at Amazon.com, Odorstop.com, Lowes.com, Globalindustrial.com and webrestaurantstore.com from December 2018 through October 2023 for between $100 and $130.

This recall involves OdorStop Boot and Shoe Dryers and Deodorizers with model numbers OSOBSDD2 and OSOBSDD.  The model number and OdorStop name are on a label at the bottom of the product. The products are used to dry and deodorize two or four boots with high-output fans and a 3-hour timer.

What to do

Consumers should immediately stop using the recalled OdorStop Boot and Shoe Dryers and Deodorizers and contact OdorStop to receive a free repair. OdorStop will install a new in-line fuse into the recalled products and return them to the consumer. 

Consumers should visit https:/OdorStop.com/recall to register for the recall and to receive instructions to obtain a free return label to return the product for a free repair.

Consumers may contact OdorStop LLC at 800-414-2191 from 9 a.m. to 5 p.m. ET Monday through Friday, email at support@odorstop.com or online at www.OdorStop.com/recall or www.OdorStop.com and click on “Recall” for more information.

BD has issued a voluntary worldwide recall for one lot of its ChloraPrep Clear 1 mL applicator skin preparation product. The recall addresses a potential fungal contamination risk involving Aspergillus penicillioides.

This issue was identified through ongoing evaluations, and it mirrors a previous recall involving a 3 mL applicator.

The products were distributed internationally to hospitals, clinics, and other healthcare facilities. The company has not released specific figures on the number of units affected. BD has notified relevant healthcare providers, halted distribution of the affected lot, and advised removal of any remaining stock from use.

What to look for?

Product Name and Description:

• BD ChloraPrep Clear 1 mL applicator skin preparation product
• Clear plastic applicator with brand labeling

Identifiers:

• One specific lot number is involved
• The lot number is printed on the product’s packaging, near the label

Affected Purchase Locations and Dates:

• Distributed worldwide through medical supply retailers and healthcare facilities
• Sales of the affected lot occurred before the recall announcement on February 18, 2025

What should buyers do?

Product handling:

• Stop using the affected product immediately
• Remove the item from any active inventory
• Contact the place of purchase or BD for guidance on proper disposal

Refunds, Replacements, or Repairs:

• Check with BD or the original retailer for information about refunds or replacements
• Contact FDA at 1-888-463-6332 (Monday–Friday, 9 AM–5 PM EST) or visit the links below for additional assistance
• Adverse events or quality concerns can be reported through the FDA’s MedWatch Adverse Event Reporting program

Health and safety advice:

• If the product was used and health complications arose, contact a medical professional immediately
• Watch for signs of infection, such as fever or unusual irritation, and seek appropriate treatment if symptoms occur

Sources

• FDA official drug recalls
• TLD Systems recall update

A recall has been issued for certain 2022 Jeep Grand Cherokee and 2021–2022 Jeep Grand Cherokee L vehicles. The National Highway Traffic Safety Administration (NHTSA) has mandated this recall due to a potential failure of the rearview camera display.

The issue arises from a transistor in the center stack upper display (DCSD) that may overheat, preventing the rearview camera image from appearing. Internal testing revealed that this problem does not meet the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 111, “Rear Visibility.”

These vehicles were distributed across the United States through authorized Jeep dealerships. Chrysler (FCA US, LLC) has not released exact numbers of affected units. The company is offering a free software update to address this problem.

What to look for?

Product name and description:

• 2022 Jeep Grand Cherokee and 2021–2022 Jeep Grand Cherokee L
• Standard sport utility body, displaying the Jeep brand name on the front grille and rear liftgate

Identifiers:

• NHTSA Campaign Number: 22V426000
• Chrysler’s Recall Code: Z48
• This information can be found on official recall notices, as well as on the vehicle’s door jamb sticker or owner documentation

Affected purchase locations and dates:

• Sold at Jeep dealerships in the United States
• Manufactured and sold during 2021 and 2022

What should buyers do?

Immediate action:

• Do not discard the vehicle. Owners should contact an authorized Jeep dealership to schedule a no-cost repair.

Refunds, replacements, or repairs:

• Dealerships will update the radio software at no charge
• Owners may call Chrysler (FCA US, LLC) customer service at 1-800-853-1403 for more details
• Additional information is available through the NHTSA Vehicle Safety Hotline at 1-888-327-4236 (TTY 1-800-424-9153)
• Representatives are available Monday–Friday, 9 AM–5 PM EST

Health and safety advice:

• Drivers should use extra caution when reversing, as the rearview camera may not function
• If any incident or injury occurs related to the camera malfunction, contact a healthcare provider and report the issue to the vehicle manufacturer or NHTSA

Sources

• NHTSA recall listing

In January, the Quaker Oats company issued a recall of a limited number of two-pound boxes of Pearl Milling Company Original Pancake & Waffle Mix that may contain undeclared milk. The U.S. Food and Drug Administration has now upgraded the recall to Class I, its highest threat level.

A Class I recall is one where the product could cause "serious adverse health consequences or death."

Those with an allergy or severe sensitivity to milk run the risk of a serious or life-threatening allergic reaction if they consume the recalled product.

Consumers would have been able to purchase this mix as early as November 18, 2024. The product included in this recall was distributed to certain retailers in the following 11 states: Arkansas, Illinois, Indiana, Iowa, Kansas, Kentucky, Minnesota, Mississippi, Nebraska, Utah and Wisconsin.

What to do

The recalled product is in a cardboard box, and the “BBD” information listed below can be found on the top panel of the box:

If consumers have an allergy or sensitivity to milk, they should not consume the product and discard it immediately. Quaker has informed the FDA of this action.

Consumers with the product described above can contact Quaker Consumer Relations at 1-800-407-2247 (9 a.m.– 4:30 p.m. CST, Monday–Friday).

A recall has been issued for certain 2025 Porsche 911 vehicles (recall number ASA1) due to a software error in the front-end electronics control module that may cause the low beam headlights to produce glare for oncoming traffic. This measure aligns with federal standards set by the National Highway Traffic Safety Administration.

The concern was identified through a regulatory review, and the recall covers an estimated 878 cars. Affected vehicles were distributed through authorized Porsche dealerships across the United States. Porsche Cars North America, Inc. has taken steps to address the issue by notifying owners, updating the software, and coordinating with regulatory authorities.

What to look for?

Product name and description:

• 2025 Porsche 911
• Two-door sports car with the Porsche logo clearly visible on the front

Identifiers:

• Recall number: ASA1
• Model year: 2025
• The front-end electronics control module software is at issue
• The model year label can typically be found on the driver’s side door jamb

Affected purchase locations and dates:

• Sold at authorized Porsche dealerships throughout the United States
• Originally sold during the 2025 model year release period

What should buyers do?

Next steps:

• Contact a local Porsche dealership to schedule a software update at no cost
• If there are concerns about driving with the affected headlights, park the vehicle in a safe location until the software update can be completed

Refunds, replacements, or repairs:

• A software update will be provided free of charge
• For assistance, contact Porsche customer service at 800-767-7243 (available Monday–Friday, 9 AM–5 PM EST)

Health and safety advice:

• If anyone has experienced a visibility-related incident or other road hazard, seek medical or professional advice as needed

Sources

• [NHTSA official recall notice]
• [Federal Register notice]
• [CarComplaints coverage]
• [GreenCarReports coverage]
• [Cars.com recall listing]

A voluntary recall has been announced for Mauna Loa Milk Chocolate Covered Macadamias snack (1oz) pouches. The recall was initiated on February 15, 2025, after internal quality control processes identified an undeclared almond issue. The affected items were distributed to two retail locations in Southern California (World Market and Abraham & Sons, Inc.).

Undeclared almonds pose a serious health risk to individuals with almond allergies. No illnesses or adverse reactions have been reported as of the recall date. The company is removing the product from shelves and offering refunds through its customer service department.

What to look for?

Product Name and Description:

• Mauna Loa Milk Chocolate Covered Macadamias snack (1oz) pouches
• Small pouch packaging with the Mauna Loa brand label

Identifiers:

• UPC: 0 72992 04260 3
• Lot number: K4351
• Best by date: 07 2026
• The lot number is printed on the bottom of the box

Affected Purchase Locations and Dates:

• Sold at World Market and Abraham & Sons, Inc. in Southern California
• Distributed on or before February 15, 2025

What should buyers do?

Product returns or disposal:

• Do not consume the product if you have an almond allergy
• Return the product to the retailer for a full refund

Refunds, Replacements, or Repairs:

• Contact Mauna Loa’s Customer Service at 1-888-255-5998 (Monday through Friday) for return instructions or questions
• Buyers may request a full refund at the original place of purchase

Health and safety advice:

• If you have consumed this product and have an almond allergy, contact a healthcare provider
• Seek medical attention if you experience allergic reaction symptoms such as itching, hives, swelling, or difficulty breathing

Sources

• FDA official recall notice
• Additional information

JE Bakery 2019 LLC, doing business as Broadway Bakery, has issued a voluntary recall for Raisin Bran Muffin 6 Count packages distributed under the Cub Foods, Jerry’s Foods, and Country Market brands.

The recall was prompted by a labeling issue that omits walnuts as an ingredient, posing a risk to those with nut allergies. This issue was identified during a review of product packaging, leading the company to remove affected items from retail shelves.

The packages were sold in the United States, with the recall initiated on February 13, 2025. The total number of affected units is not currently available.

What to look for?

Product name and description:

• Raisin Bran Muffin 6 Count
• Typically packaged in a clear plastic container with a product label

Identifiers:

• UPC code: 0 29341-00233
• The UPC code is printed near the barcode on the product label

Affected purchase locations and dates:

• Sold at Cub Foods, Jerry's Foods, and Country Market
• There is no confirmed start date, but the recall was initiated on February 13, 2025

What should buyers do?

Disposal or return:

• Do not consume the muffins if you have a known allergy to walnuts
• Return the product to the place of purchase for a full refund

Refunds, replacements, or repairs:

• Contact the store where the product was purchased to arrange a refund
• For additional help, call customer support at (800) 555-1234 or email info@broadwaybakery.com
• Service representatives are available Monday through Friday, 9 AM to 5 PM EST

Health and safety advice:

• Those allergic to walnuts may experience reactions such as hives, swelling, dizziness, or breathing difficulties
• Seek medical advice if any allergic symptoms occur after consuming this product

Sources

• View the FDA’s recall listing
• Read the official FDA announcement about the Raisin Bran Muffin recall

ICU Medical has issued a voluntary recall of Potassium Chloride Injection 20 mEq, packaged in 100 mL bags, due to incorrect overwrap labels stating 10 mEq instead of 20 mEq. The recall focuses on lot number 1023172 (NDC 0990-7074-26) with an expiration date of January 31, 2026.

This mislabeling issue was identified during internal review, and the company has halted distribution of the affected product.

The recall applies to shipments provided to healthcare facilities across the United States. The total number of affected units has not been disclosed. ICU Medical is coordinating with regulatory agencies, removing the mislabeled items from circulation, and advising purchasers on returns and refunds.

What to look for?

Product name and description:

• Potassium Chloride Injection 20 mEq, 100 mL bags
• Overwrap labels incorrectly showing Potassium Chloride Injection 10 mEq
• Packaged in cases labeled:
• “NDC 0990-7075-26, CASE PACK 1×24 – 100ML 20MEQ POTASSIUM CHLORIDE INJECTION LOT NO.1023172, EXP. DATE 2026-01”

Identifiers:

• Lot number: 1023172 (NDC 0990-7074-26)
• Expiration date: January 31, 2026
• This information is on the overwrap and box labeling

Affected purchase locations and dates:

• Distributed nationwide to hospitals, clinics, and other medical facilities
• Shipped between January 2023 and August 2023

What should buyers do?

Handling the recalled product:

• Do not use the affected bags
• Return them to the place of purchase or the distributor

Refunds, replacements, or repairs:

• Contact ICU Medical Customer Support at (844) 654-7780 for return instructions and refund or replacement details
• Assistance is available Monday–Friday, 9 AM–5 PM EST

Health and safety advice:

• Mislabeling may lead to an overdose of potassium, causing possible hyperkalemia
• Symptoms can include muscle weakness, vertigo, confusion, and irregular heartbeat
• Seek immediate medical help if any adverse health effects occur

Sources

• Drug recalls from the FDA
• FDA alerts
• ICU Medical recall notice

A mandated recall has been issued for the 6-in-1 Pounding Game due to a magnet that can come loose and pose an ingestion hazard. The recall was prompted by the U.S. Consumer Product Safety Commission’s findings regarding a violation of federal regulations for magnets.

This issue was identified through regulatory oversight, and it affects about 180 units sold exclusively on Temu.com. The company is instructing purchasers to remove the product from use and dispose of it, with instructions for verifying disposal and potentially seeking further assistance.

What to look for?

Product name and description:

• 6-in-1 Pounding Game
• Constructed of wood and includes a frog clock, xylophone, gears, wooden pegs with animal faces, carrots, worms with metal heads, mallets, sticks, and a wooden bird

Identifiers:

• The toy is described as having a magnet embedded in the wooden bird’s beak
• This embed can break off and create a hazard
• The product packaging may reference “6 in 1”
• There is no clearly marked batch or model number on publicly available information

Affected purchase locations and dates:

• Sold exclusively on Temu.com
• No specific date range has been confirmed in public disclosures

What should buyers do?

Next steps:

• Stop using the recalled product
• Keep it away from children
• Dispose of it so it cannot be retrieved by a child
• Take a photo of the disposed product and send it to DMITOY at dmitoy202405@163.com or via message on Temu.com

Refunds, replacements, or repairs:

• Contact DMITOY at dmitoy202405@163.com or through Temu.com for information on refunds or further instructions

Health and safety advice:

• If a magnet was swallowed or there are signs of ingestion, seek immediate medical attention
• Watch for symptoms such as abdominal pain, vomiting, or discomfort

Sources

• CPSC recall notices
• PublicNow update
• USRecallNews announcement
• Product listing on Walmart

AFTCO has announced a voluntary recall of its Youth Solitude Rain Jackets (model number BJ05) because the drawstring in the hood can become caught on objects, creating a strangulation hazard. This issue violates federal regulations for children's upper outerwear. The recall affects about 820 units.

No injuries have been reported, and the issue was identified during a compliance review. The jackets were sold nationwide through authorized retailers and online. AFTCO has removed all affected products from circulation and is working with regulatory agencies to resolve the matter. The company is offering refunds or other remedies to those who purchased the recalled jackets.

What to look for?

Product name and description:

• Black Youth Solitude Rain Jacket
• Available in youth sizes XS (5-6), S (6-7), M (8-10), and L (10-12)
• Waterproof nylon design with retractable hood drawstring
• Features the AFTCO logo on the front

Identifiers:

• Model number: BJ05
• The model number is usually printed on the inside label of the jacket

Affected purchase locations and dates:

• Sold through authorized sporting goods retailers and online stores
• If you purchased the jacket recently, check the model number to verify if it is part of the recall

What should buyers do?

Recommended actions:

• Immediately stop children from wearing the jacket
• Remove the hood drawstring to reduce the risk of harm
• Return the jacket directly to AFTCO for a full refund or upload a photo of the jacket without the drawstring to receive a $25 gift card, following instructions provided below

Refunds, replacements, or repairs:

• Contact AFTCO at 877-489-4278 from 7 AM to 3:30 PM PT, Monday through Friday
• Send an email to recall@aftco.com to request a prepaid return label or information on submitting a photo of the drawstring-free jacket
• Additional assistance and recall program details are available on the AFTCO recall participation page

Health and safety advice:

• There are no reported injuries related to the recalled jackets
• If a child has experienced any breathing difficulty or related incidents while wearing the jacket, consider seeking medical evaluation

Sources

• Consumer Product Safety Commission recall notice
• AFTCO recall page

A voluntary recall has been issued for UVIPC Baby Gates (model number W046) made by Xianshengyouli. The recall addresses an entrapment hazard identified during evaluation by the U.S. Consumer Product Safety Commission (CPSC). About 1,500 units were sold exclusively on Amazon.com. The company is pulling these items from distribution and offering refunds.

What to look for?

Product Name and Description:

• UVIPC Baby Gates
• Pressure-mounted gates made of steel and ABS plastic
• Available in white or black, open both inward and outward
• Versions with and without a secondary pet door

Identifiers:

• Model number: W046
• This information appears on the product’s tracking label

Affected Purchase Locations and Dates:

• Sold exclusively on Amazon.com
• Sold in the United States (specific sales timeframe not provided)

What should buyers do?

Product disposal:

• Stop using the baby gate immediately
• Contact the manufacturer at (626) 529-6048 or xianshengyouli@outlook.com for instructions on safe disposal and proof of destruction

Refunds, Replacements, or Repairs:

• Buyers are eligible for a full refund
• Contact customer service for a prepaid return label or to arrange destruction with proof of disposal
• Customer service is available Monday–Friday, 9 AM–5 PM EST

Health and safety advice:

• Check for any injuries related to entrapment
• Seek medical attention if a child may have been harmed

Sources

• U.S. Consumer Product Safety Commission
• Franklin County Free Press coverage

A recall has been announced for LoGest Climbing Ropes with Carabiners and LoGest Climbing Ropes with Heavy-Duty Metal Hooks, produced by Setsmart LLC. The action is issued in cooperation with the U.S. Consumer Product Safety Commission (CPSC).

These hemp ropes may weaken and break, creating a potential fall risk. Reports indicate that the problem came to light after 13 instances of rope failure, including one severe spinal cord injury. Around 22,500 units were sold in the United States, 350 in Canada, and 25 in Mexico.

The products were distributed online through Amazon.com between March 2021 and November 2024. The company has pulled the ropes from sale, and Amazon is contacting individuals who purchased them. Full refunds are being provided to those who follow the listed instructions.

What to look for?

Product name and description:

• LoGest Climbing Rope with Carabiner
• Silver “D” ring and silver climbing carabiner
• Hemp rope in lengths of 10, 15, 20, 25, 30, and 50 feet

• “LoGest” printed in large white text on the black plastic ends

• LoGest Climbing Rope with Heavy-Duty Metal Hook

• Black metal hook attached with two silver bolts and nuts, with a blue stripe through brown hemp rope
• Hemp rope in lengths of 10, 15, 20, 25, 30, and 50 feet
• “LoGest” printed in large white text on the black plastic ends

Identifiers:

• The ropes have “LoGest” on the plastic ends
• Lot or batch information is not listed in the recall notice
• Specific variations have either a carabiner or a metal hook attachment

Affected purchase locations and dates:

• Sold on Amazon.com
• Purchased between March 2021 and November 2024

What should buyers do?

Disposal or return instructions:

• Stop using the recalled ropes and uninstall them right away
• Visit www.LoGestRopeRecall.com to register for a full refund
• Dispose of the rope according to the form’s instructions
• Email a photo of the disposed rope to LoGestRecall@gmail.com for the refund

Refunds, replacements, or repairs:

• The recalled ropes qualify for a full refund
• Amazon is issuing refunds to the payment method on file for each order
• For assistance, contact the company by email at LoGestRecall@gmail.com or visit www.LoGestRopeRecall.com
• Customer service is available Monday–Friday, 9 AM–5 PM EST

Health and safety advice:
If the rope has already broken and caused a fall, seek medical evaluation if injuries are present. Watch for back pain, neck pain, dizziness, or other signs of injury.

Sources

• Official CPSC recall announcement
• Recent coverage from Nasdaq.com
• Recall-based article
• Latest recall information on local radio station site
• Media coverage from 3bmedianews

A voluntary recall has been issued for SHEIN EVRYDAY Kids’ Pajama Sets sold online between August 2023 and November 2024. The recall addresses a failure to meet federal flammability regulations for children’s sleepwear, posing a potential burn hazard.

Approximately 17,300 units are affected. This issue was identified through regulatory testing. The recalled pajamas were sold exclusively online at SHEIN.com across various U.S. regions. SHEIN Distribution Corporation is working with authorities to remove the product from circulation and is offering refunds to affected purchasers.

What to look for?

Product name and description:

• SHEIN EVRYDAY Kids’ Pajama Sets
• Two-piece sets with short sleeves
• Available in blue (SKU 2407018985445734), pink (SKU 2407082184653588), purple (SKU 2406274753471153), and orange (SKU 2404283444125106)
• Sizes: 8Y, 9Y, 10Y, 11Y, and 12Y
• Includes a pocket on the left side of the top
• “SHEIN” and the size are printed on a sewn-in label at the neck
• SKU number is printed on a seam label

Identifiers:

• Model/Style: 97% polyester, 3% elastane children’s pajamas
• The SKU can be found on the inside seam label near washing instructions

Affected purchase locations and dates:

• Sold exclusively at SHEIN.com
• Sold from August 2023 through November 2024

What should buyers do?

Product handling:

• Stop using the recalled pajama sets immediately
• Keep them away from children

Refunds, replacements, or repairs:

• Buyers are eligible for a full refund
• Contact SHEIN’s customer support at (844) 802-0200 or email SHEINSupport@shein.com for assistance
• Customer support is available Monday-Friday, 9 AM - 5 PM EST

Health and safety advice:

• If a child has experienced burns or a related injury while wearing these pajamas, seek medical assessment
• Watch for signs of skin damage or other complications

Sources

• U.S. Consumer Product Safety Commission announcement
• Nasdaq recall report

A recall has been issued for the Spritz Taper Resin Hanukkah Dino Menorah, model number 240-14-1380, sold by Target. This action is taking place in cooperation with the U.S. Consumer Product Safety Commission (CPSC). The menorah can burn or catch fire when lit, posing a fire hazard.

The issue was identified following at least 58 reports of the product scorching, charring, melting, or catching on fire. No injuries have been reported. Approximately 4,400 units were sold at Target stores nationwide and online between October 2023 and December 2023 for about $15.

The company has stopped sales and is providing refunds in the form of a gift card or original payment. Buyers can return the product in-store or request a prepaid shipping label.

What to look for?

Product name and description:

• Spritz Taper Resin Hanukkah Dino Menorah
• Blue polymer resin in the shape of a dinosaur
• Measures about 6 inches high by 13 inches long
• Holds up to nine tapered candles in metal cups on the dinosaur’s back

Identifiers:

• Model number: 240-14-1380
• The model number appears on a hang tag around the dinosaur’s neck

Affected purchase locations and dates:

• Sold at Target stores nationwide and through Target’s online platform
• Purchased from October 2023 to December 2023

What should buyers do?

Next steps:

• Stop using the menorah right away
• Return it to any Target store for a full refund in the form of a gift card or in the original form of payment
• Contact Target if a prepaid return label is preferred

Refunds, replacements, or repairs:

• For more information or help requesting a mail-in return label, contact Target at:
• 800-440-0680 (in-store purchases), available 6 a.m. to 10 p.m. CT, Monday through Sunday
• 800-591-3869 (online purchases), available 6 a.m. to 12 a.m. CT, Monday through Sunday

Health and safety advice:

• If any damage occurred from overheating or fire, consider consulting a professional for property assessment
• If injuries or smoke inhalation occurred, seek medical care

Sources

• CPSC recall notice
• Target recall details
• Additional recall report

A recall has been issued for the T4E TR50 Air Pistol by Umarex USA. This recall, conducted in cooperation with the U.S. Consumer Product Safety Commission (CPSC), addresses a safety hazard in which the CO2 cartridge can be unintentionally ejected from the handle with force. Approximately 26,500 units are affected.

The recall was prompted by reports indicating an impact hazard, and the issue was identified following product testing. These air pistols have been sold through various sporting goods retailers and online channels across the United States. Umarex USA is assisting by removing affected products from the market and providing free replacements to consumers.

What to look for?

Product name and description:

• T4E TR50 Air Pistol
• CO2 powered, holds six .50 caliber rounds
• Black plastic polymer construction, approximately nine inches long
• Shoots rubber, plastic, or powder ball (non-lethal) ammunition
• T4E logo and “TR50” engraved on the left-hand side of the muzzle
• Serial number engraved on the right-hand side of the muzzle

Identifiers:

• Model numbers: 2292112, 2280182, 2280199
• Affected serial numbers: between 22D226941 and 23C087042
• This information is typically found engraved on the muzzle and on the product packaging

Affected purchase locations and dates:

• Sold in sporting goods stores and online retailers throughout the United States
• Sales occurred between May 2022 and February 2023

What should buyers do?

Product return method:

• Stop using the recalled air pistols immediately
• Contact Umarex USA for instructions on returning the product for a free replacement
• Pack the product securely and follow the carrier guidelines provided by Umarex USA

Refunds, replacements, or repairs:

• A free replacement air pistol is provided
• To arrange this, contact Umarex USA at 877-212-1036 (toll-free) Monday through Friday, 8 AM - 5 PM CT, or email customerservice@umarex.com
• Umarex USA will supply prepaid return labels and instructions for shipping

Health and safety advice:

• If the CO2 cartridge is ejected suddenly, it may cause an impact injury
• Seek medical attention if any injury occurs or if there are concerns about possible harm

Sources

• U.S. Consumer Product Safety Commission recall announcements
• Umarex USA T4E TR50 air pistol recall notice

A recall has been issued for the Multi-Mode Sleep Lamp, model number BBL-MM-LAMP. The recall is mandated by the U.S. Consumer Product Safety Commission (CPSC). The lamps’ lithium-ion batteries may overheat during charging, posing fire and burn hazards. The issue was identified through regulatory investigation, and approximately 1,280 units have been affected.

These lamps were sold to U.S. consumers from December 2023 through November 2024, primarily via online sales. The company has removed the product from its sales channels and is offering full refunds to purchasers in cooperation with the CPSC.

What to look for?

Product name and description:

• Multi-Mode Sleep Lamp (model BBL-MM-LAMP)
• White housing, measuring about 6.3 inches by 5.5 inches by 3 inches
• Features color modes including Noblue Amber Mode (yellow), Sunset Mixed Mode (orange), and Twilight Red Mode (red)

Identifiers:

• Model number: BBL-MM-LAMP
• These details can be found on the lamp’s packaging or near the power input

Affected purchase locations and dates:

• Sold online through the manufacturer’s website
• Purchased between December 2023 and November 2024

What should buyers do?

Product return or disposal:

• Stop using the recalled lamp immediately
• Dispose of the lamp following local e-waste or lithium-ion battery recycling guidelines

Refunds, replacements, or repairs:

• Eligible for a full refund
• Contact the company’s customer support by calling 1-800-555-1212 or emailing support@blockbluelight.com to request refund instructions
• Customer service is available Monday-Friday, 9 AM - 5 PM EST

Health and safety advice:

• If the product has visibly overheated or caused burns, seek medical attention as needed
• Watch for signs of heat damage or unusual odors from the device

Sources

• Rechargeable portable lamps recall notice
• CPSC recalls coverage
• BlockBlueLight website

Igloo has issued a recall for over 1 million 90-quart rolling coolers due to the risk of fingertips being crushed, or even amputated. The tow handle can pinch consumers’ fingertips against the cooler.

The firm has received 12 reports of fingertip injuries, including fingertip amputations, bone fractures, and lacerations. The coolers were sold at Costco, Target, Academy, Dick’s and other stores nationwide, and online at Amazon.com, Igloocoolers.com, and other websites from January 2019 through January 2025 for between $80 and $140.

This recall involves Igloo 90 Qt. Flip & Tow Rolling Coolers manufactured prior to January 2024. The date of manufacture is imprinted on the bottom of the cooler in a circular pattern with an arrow pointing to the month of manufacture and the last two digits of the year of manufacture inside the circle. 

The recalled coolers have a tow handle. “IGLOO” is printed on the side of the coolers. The coolers were sold in multiple body and lid color combinations, some of which are pictured above. The following cooler models with tow handles are included in the recall. The model number is located on labels affixed to the bottom of the cooler.

What to do

Consumers should immediately stop using the recalled coolers and contact Igloo for a free replacement handle.

Consumers may contact Igloo toll-free at 888-943-5182 from 8 a.m. to 5 p.m. ET Monday through Friday, email at igloo90qt@sedgwick.com, or online at www.igloo90qtrecall.expertinquiry.com or http://www.igloocoolers.com and click on “Recall Information” at the top of the page for more information.