Recalls in March 2025

Cargill Kitchen Solutions, a unit of farming giant Cargill, is recalling around 212,268 pounds of egg beaters because they can contain bleach, the U.S. Department of Agriculture said late Friday.

After receiving a tip about potential contamination, USDA's Food Safety and Inspection Service investigation determined the egg beaters, which include the brand Bob Evans, could be contaminated with sodium hypochlorite, commonly known as bleach.

Produced between March 12 and March 13, the recalled egg beaters shipped to distributors in Ohio and Texas and for foodservice use in Arizona, California, Colorado, Florida, Illinois and Iowa, "but there is a possibility that the products were distributed nationwide," the USDA said.

The USDA said it "is concerned that some product may be in consumers’ or foodservice refrigerators or freezers."

Still, the USDA said it "does not expect any adverse health effects" from the egg beaters containing bleach and there have been no "confirmed reports" of bad reactions from eating them.

Here's the list of the recalled egg beaters:

• 32-oz. (2-lb.) carton containing “egg beaters ORIGINAL LIQUID EGG SUBSTITUTE” and USE BY AUG 10 2025.
• 32-oz. (2-lb.) carton containing “egg beaters CAGE-FREE ORIGINAL LIQUID EGG SUBSTITUTE” and USE BY AUG 09 2025.
• 32-oz. (2-lb.) carton containing “egg beaters CAGE-FREE ORIGINAL FROZEN EGG SUBSTITUTE” and “egg beaters NO ENJAULADAS ORIGINAL SUSTITUTO DE HUEVO CONGELADO” and USE BY MAR 07 2026.
• 32-oz. (2-lb.) carton containing “Bob Evans Better’n Eggs Made with Real Egg Whites” and USE BY AUG 10 2025.

What to do

The recalled egg beaters should be thrown away or returned to the place of purchase, the USDA said.

Buyers of the egg beaters with questions should contact Cargill Kitchen Solutions at 1-844-419-1574 or media@cargill.com.

The Bakery Group of Dallas, Texas, has issued a voluntary recall for certain brioche products, including 629 cases of Dense Brioche Pullman Loaves (product code 654203) and 104 cases of 4.5-inch Brioche Hamburger Buns (product code 54500). The affected items contain undeclared milk, soy, and Yellow FD&C #5 (tartrazine), which can pose risks to those allergic or sensitive to these ingredients.

This recall follows a routine inspection by Texas Health and Human Services that identified missing allergen statements on the product labels. The products were distributed between December 24, 2024, and March 12, 2025, to retail outlets such as Ben E. Keith in Fort Worth, Texas, and Rodeo Goat Casa Linda in Dallas, Texas. The company, working with the FDA, is removing the products from circulation and offering refunds or relabeling options for those impacted. No illnesses or allergic reactions have been reported at this time.

What to look for?

Product name and description:

• Dense Brioche Pullman Loaves (product code 654203)
• 4.5-inch Brioche Hamburger Buns (product code 54500)
  The products come in brown boxes labeled with either Ben E. Keith or Rodeo Goat Casa Linda brand information.

Identifiers:

• The product codes listed above are found on the outer packaging
• Missing allergen statements on the label

Affected purchase locations and dates:

• Distributed to Ben E. Keith in Fort Worth, Texas, and Rodeo Goat Casa Linda in Dallas, Texas
• Sold between December 24, 2024, and March 12, 2025

What should buyers do?

Handling of the product:

• Do not consume these products if you are allergic or sensitive to milk, soy, or FD&C Yellow #5
• Return them to the place of purchase or contact The Bakery Group for relabeling or a refund

Refunds, replacements, or repairs:

• Buyers can request a refund or updated labeling
• Contact The Bakery Group at 1-800-555-1234 or email recall@thebakerygroup.com for more information
• Customer support is available Monday-Friday, 9 AM - 5 PM EST

Health and safety advice:

• Individuals who experience symptoms such as hives, swelling, or difficulty breathing after consuming these products should seek medical attention
• No confirmed cases of adverse reactions have been reported to date

Sources

• FDA recall announcement
• Foodsafetynews coverage
• Source86 coverage
• Food Poisoning Bulletin coverage
• Karmactive coverage

Specialized Bicycle Components is recalling 32,400 of its Specialized Vado and Como IGH E-Bikes because the protective guard doesn't cover the belt drive, meaning loose clothing can get caught in and cause falls, the Consumer Product Safety Commission said Thursday.

No injuries were reported.

The recalled bikes sold at authorized retailers nationwide and online from March 2021 through November 2024 for between $3,250 and $5,750, the CPSC said.

The recall covers fifteen models of bikes. Below is a table with the recalled Specialized bikes.

What to do

Buyers should stop using the bikes and go to the nearest authorized Specialized retailer for a free repair, the CPSC said.

Specialized can be reached at 1-877-808-8154 from 8 a.m. to 4 p.m. MT Monday through Friday, by email at ridercare@specialized.com or online at http://www.specialized.com/safety-recall-notices.

Specialized is also contacting all known purchasers.

About 28,590 GIKPAL dressers are being recalled because they can tip over on young children. The dressers were sold exclusively on Walmart.com by ONME Direct.

The recalled dressers are unstable if they are not anchored to the wall, posing serious tip-over and entrapment hazards that can result in injuries or death to children. The dressers violate the performance and labeling requirements of the STURDY Act.

This recall involves GIKPAL 10 drawer dressers with model number HI1318_13. The dressers were sold in rustic brown with black handles and black sides and back. The dressers measure about 11.8 inches wide, 38.9 inches long and 39.4 inches tall, and weigh about 36 pounds. The model number “HI1318_13,” “Fabric Dresser” and “Made in China” are printed on the product packaging.

What to do

Consumers should immediately stop using the recalled dressers if they are not properly anchored to a wall and place them in an area that children cannot access. Contact ONME Direct for instructions to receive a full refund and submit a photo of the consumer disposing of the product to onmeus@outlook.com. ONME Direct and Walmart are contacting all known purchasers directly.

Consumers may contact ONME Direct toll-free at 833-449-5777 from 9 a.m. to 6 p.m. PT Monday through Friday, email at onmeus@outlook.com, or online at https://onmeus.com/pages/recall-1 or https://onmeus.com and click “Recall” at the top of the page for more information.

Segway has issued a recall for 220,000 Segway Ninebot Max G30P and Max G30LP KickScooters because The folding mechanism can fail and cause the handlebars or stem to fold while the scooter is in use, posing a fall hazard to riders.

Segway has received 68 reports of folding mechanism failures, including 20 injuries to include abrasions, bruises, lacerations and broken bones. The scooters were sold at Best Buy, Costco, Walmart, Target and Sam’s Club nationwide and online at Segway.com and Amazon.com from January 2020 through February 2025 for between $600 and $1,000.

This recall involves all Segway Ninebot Max G30P and Max G30LP KickScooters. The Max G30LP KickScooter is gray in color with yellow accents and the Max G30P is black in color with yellow accents. 

The brand name “ninebot” appears on the foot platform and the top of the handlebars. The model number is located on a label on the side of the foot deck. The Max G30P model is 46 inches long, 19 inches wide, 47 inches high and weighs 42 pounds. The Max G30LP model is 44 inches long, 19 inches wide, 45 inches high and weighs 39 pounds.

What to do

Consumers should immediately stop using the recalled scooters and contact Segway to receive information to determine whether the folding mechanism needs adjustment and to receive a free maintenance kit. The kit includes tools and instructions for checking and tightening the folding mechanism and keeping it properly maintained.

Consumers may contact Segway at 800-914-6110 from 9 a.m. to 5 p.m. Monday through Friday, email at recall@segway.com, or online at https://service.segway.com/recall or www.segway.com, and click on “Recall Center” at the bottom of the page for more information.

Sensio has issued a recall for about 12,300 steam espresso machines due to burn and laceration hazards. The brew cup handle can forcefully eject during use, shattering the glass carafe and posing a burn and laceration hazard.

The firm has received 18 reports of the handles ejecting, eight of which reported burn and/or laceration injuries. The machines were sold at JCPenney stores nationwide and online at BestBuy.com and JCPenney.com from August 2023 through January 2025 for between $40 and $60.

This recall involves the Bella Pro Series Steam Espresso Maker, Model 90195 and Cooks Steam Espresso Makers, Model 22395. The recalled espresso machines are black with stainless steel trim and measure about six inches wide and 12 inches high. The machines have “Bella Pro Series” or “Cooks” on the steaming chamber and the model number is identified as the “Item” number on a sticker under the machine.

What to do

Consumers should immediately stop using the recalled espresso machines and contact Sensio for a refund.

Contact Sensio toll-free at 855-647-3125 from 8 a.m. to 5 p.m. ET Monday through Friday or online at www.bellakitchenware.com and click on “Recalls” for more information.

The Food and Drug Administration (FDA) has announced the voluntary recall of several popular acne products due to high levels of benzene. 

The chemical is used in the production of products like dyes, detergents, and some plastics, and  it’s also emitted into the air by cigarette smoke. However, exposure to benzene comes with health risks. 

“The health consequences of benzene exposure depend on the amount, route, and length of time of exposure, as well as age and preexisting medical conditions of the product user,” the FDA explained. 

“In small amounts over long periods of time, benzene can decrease the formation of blood cells. Long-term exposure to benzene through inhalation, oral intake, and skin absorption may result in cancers such as leukemia and other blood disorders.” 

What products are recalled?

The FDA conducted independent testing of nearly 100 popular acne products to determine the levels of benzene of products currently on store shelves. 

While over 90% of the products tested were safe, there were some products with benzoyl peroxide that translated to unsafe levels of benzene.  

Here’s a look at the affected products: 

• La Roche-Posay Effaclar Duo Dual Action Acne Treatment

  • Lot Number: MYX46W    

  • Expiration Date: April 2025

• Walgreens Acne Control Cleanser    

  • Lot Number: 23 09328    

  • Expiration Date: September 2025

• Proactiv Emergency Blemish Relief Cream Benzoyl Peroxide 5%    

  • Lot Number: V3305A; V3304A    

  • Expiration Date: October 2025

• Proactiv Skin Smoothing Exfoliator    

  • Lot Number: V4204A

  • Expiration Date: July 2025

• SLMD Benzoyl Peroxide Acne Lotion    

  • Lot Number: 2430600

  • Expiration Date: March 2025

• Walgreens Tinted Acne Treatment Cream    

  • Lot Number: 49707430

  • Expiration Date: March 2026

Another product to look out for is Zapzyt Acne Treatment Gel. The manufacturer issued its own voluntary recall of the product due to high benzene levels, independent of the FDA’s investigation.  

At this time, this recall is directed to retailers, meaning these products should be removed from store shelves. However, the FDA doesn’t have any specific instructions for consumers discontinuing personal use. 

It is important to note that the FDA encourages consumers to diligently check the expiration dates on all of their skincare products and dispose of any that have expired. 

Nestlé USA has issued a voluntary recall for select batches of Lean Cuisine and STOUFFER'S frozen meals due to a potential contamination with wood-like material. The recall was prompted by a consumer report of a possible choking incident, and the company is collaborating with the U.S. Food & Drug Administration (FDA) and the U.S. Department of Agriculture (USDA).

The recalled products were produced between August 2024 and March 2025 and distributed to major retailers across the United States from September 2024 to March 2025. At this time, the total number of affected units has not been publicly released. Nestlé USA has removed the products from sale and is offering refunds or replacements.

What to look for?

Product name and description:

• Lean Cuisine Butternut Squash Ravioli

• Lean Cuisine Spinach Artichoke Ravioli

• Lean Cuisine Lemon Garlic Shrimp Stir Fry

• STOUFFER'S Party Size Chicken Lasagna (96oz)

All items are frozen meals packaged in boxes or trays bearing the Lean Cuisine or STOUFFER'S brand name.

Identifiers:

• The lot numbers and best-before dates are printed on the product packaging

• Affected Lean Cuisine codes include: 4261595912 (OCT2025), 4283595912 (NOV2025), 4356595912 (JAN2026), 5018595912 (FEB2026), 5038595912 (MAR2026), and 4214595511 (SEPT2025)

• Affected STOUFFER'S codes include: 4262595915 (OCT2025), 4351595915 (JAN2026), 5051595915 (MAR2026), 5052595915 (MAR2026)

Affected purchase locations and dates:

• Distributed to major retailers throughout the United States

• Sold between September 2024 and March 2025

What should buyers do?

Product handling:

• Do not consume the affected meals

• Return them to the place of purchase for a full refund or replacement

• If discarding, follow local waste guidelines

Refunds, replacements, or repairs:

• Contact Nestlé USA at (800) 681-1676 for information on refunds or replacements

• Phone lines are open Monday–Friday, 9 AM–6 PM EST

Health and safety advice:

• If anyone has experienced symptoms such as gagging or choking after consuming these meals, consider seeking medical attention

• Watch for continued breathing difficulty or persistent throat irritation

Sources

• FDA voluntary recall notice

• Press release from Nestlé USA

Gerolsteiner has initiated a voluntary recall of its 750ml Sparkling Natural Mineral Water sold under specific lot numbers. The recall addresses a potential laceration hazard associated with cracking glass bottles.

These products were distributed through Trader Joe’s stores across 12 states (Alabama, Arkansas, Colorado, Florida, Georgia, Kansas, Louisiana, New Mexico, Oklahoma, South Carolina, Tennessee, and Texas). Approximately 61,500 bottles are affected. Gerolsteiner is working with authorities and has removed the products from store shelves.

What to look for?

Product name and description:

• Gerolsteiner Sparkling Natural Mineral Water (750ml glass bottles)
• White, blue, and red label featuring “Gerolsteiner” branding

Identifiers:

• Lot numbers: 11/28/2024 L or 11/27/2024 L
• Lot information printed on the lower part of the label

Affected purchase locations and dates:

• Sold at Trader Joe’s in Alabama, Arkansas, Colorado, Florida, Georgia, Kansas, Louisiana, New Mexico, Oklahoma, South Carolina, Tennessee, and Texas
• Purchased between December 2024 and January 2025

What should buyers do?

Handling the product:

• Stop using and do not consume the affected water
• Return bottles to the place of purchase for a refund

Refunds, replacements, or repairs:

• Contact Gerolsteiner’s customer service at 800-777-0633 (available Monday–Friday, 8:30 AM–5 PM ET) or email customerservice@consup.us for more information
• A refund is provided upon return of the product

Health and safety advice:

• No injuries have been reported. If any lacerations occur, seek medical attention as needed

Sources

• U.S. Consumer Product Safety Commission recall notice
• Local news coverage
• Recipe site coverage

Dr. Reddy’s Laboratories has initiated a voluntary recall of Levetiracetam in 0.75% Sodium Chloride Injection (1,000 mg/100 mL), identified as Lot Number A1540076. The issue involves mislabeling of infusion bags that were incorrectly marked as containing 500 mg/100 mL of the medication rather than 1,000 mg/100 mL.

This discrepancy may lead to the administration of double the intended dose. The problem was identified after distribution, prompting a nationwide recall. The affected infusion bags were shipped between November 4 and November 6, 2024, through hospitals, pharmacies, and distributors across the United States. The company has not reported any adverse events at this time. As part of the recall, the product is being removed from circulation, and replacements or refunds are being offered to impacted purchasers.

What to look for?

Product name and description:

• Levetiracetam in 0.75% Sodium Chloride Injection (1,000 mg/100 mL)
• Packaged in infusion bags labeled incorrectly as Levetiracetam in 0.82% Sodium Chloride Injection (500 mg/100 mL)

Identifiers:

• Lot Number: A1540076
• The lot number is printed on the infusion bag’s label
• Correct strength is 1,000 mg/100 mL, despite the 500 mg/100 mL labeling

Affected purchase locations and dates:

• Distributed nationwide through hospitals, pharmacies, and medical distributors
• Shipped from November 4, 2024, through November 6, 2024

What should buyers do?

Product handling:

• Return the affected infusion bags to the original purchase source or follow the instructions provided by Dr. Reddy’s Laboratories
• Do not administer the mislabeled product under any circumstance

Refunds, replacements, or repairs:

• Contact Inmar for a prepaid return label or refund at 1-877-645-1584
• Customer service is available Monday through Friday from 9 AM to 5 PM EST

Health and safety advice:

• Seek medical attention if you believe you or someone under your care has received the mislabeled medication
• Watch for potential adverse effects such as dizziness, somnolence, respiratory issues, or other indications of overdose

Sources

• FDA recall notice
• Business Wire announcement
• CNBC TV18 coverage
• Stock Titan notice
• NDTV Profit article

A recall has been issued for retractable safety mesh gates marketed for child or pet use under model number SG021. The recall is being conducted in coordination with the U.S. Consumer Product Safety Commission.

The entrapment hazard was identified when safety testing revealed that a child’s torso could fit through the opening between the gate and the floor. Approximately 880 units have been affected. These gates were sold on Amazon from September 2024 to January 2025. The company is removing the product from the market and offering full refunds.

What to look for?

Product name and description:

• Retractable safety gates labeled as “Retractable Safety Gate” with model SG021
• Colors: white, gray, and black
• Height: about 34 inches, adjustable up to around 55 inches in width
• Frame made of aluminum
• A white label inside the frame near the handles shows the product name and model

Identifiers:

• Model number SG021 printed on the label near the handles
• Look for the text “Retractable Safety Gate” on the gate’s frame
• The label with this information is placed inside the frame near the handles

Affected purchase locations and dates:

• Sold exclusively on Amazon
• Purchased between September 2024 and January 2025

What should buyers do?

Use or disposal advice:

• Stop using the recalled gate immediately
• Destroy it by cutting the mesh
• Dispose of it following local waste guidelines

Refunds, replacements, or repairs:

• A full refund is available
• Contact the company by phone at 771-232-2236 from 10 a.m. to 4 p.m. ET, Monday through Friday
• Email support at [email protected]
• Provide a photo of the destroyed gate to receive instructions for the refund

Health and safety advice:

• No injuries have been reported
• If a child has experienced any incident related to the recalled gate, seek medical attention for potential torso or neck injuries
• Monitor for bruising, discomfort, or trouble breathing

Sources

• CPSC official recall notice
• News announcement

A voluntary recall has been issued for all BMC Kaius 01 bicycles and framesets, including those with a V5 fork. The recall stems from a potential fall hazard caused by the fork steerer tube, which can crack or separate during use.

The issue surfaced after reports of steerers coming loose, though no injuries have been reported. About 10,000 units are affected and were distributed by BMC USA Corporation. They were sold through authorized BMC dealers across various regions. BMC is removing the products from circulation and offering free replacement forks to those affected.

What to look for?

Product name and description:

• BMC Kaius 01 bicycles and framesets
• Offered in Peacock Spider, Carbon Black/Brushed Blue, Purple/White, White/Black, Turquoise/Black, Saffron/Black, and Stone Grey
• The brand name “BMC” is printed on the downtube

Identifiers:

• V5 fork
• Manufacturing details found on the original label near the fork steerer tube
• Owners may locate the model name and branding on the bike frame

Affected purchase locations and dates:

• Sold through authorized BMC dealers
• Records indicate sales leading up to the recall date of March 13, 2025

What should buyers do?

Instructions for buyers:

• Stop using the recalled bicycles or framesets
• Contact an authorized BMC dealer for guidance on free inspection and fork replacement

Refunds, replacements, or repairs:

• A free fork replacement is available
• Contact the company by phone at 888-262-7755 from 9 AM to 5 PM PT, Monday through Friday
• Email kaius-fork-recall-USA@BMC-Switzerland.com for a prepaid return label if needed
• Visit the BMC website for more assistance if the purchase history is unclear

Health and safety advice:

• If anyone experiences a fork failure while riding, watch for injuries such as bruises or fractures
• Seek medical evaluation if any concerning symptoms arise from a fall or accident

Sources

• U.S. Consumer Product Safety Commission
• BMC voluntary recall notice

Sublue has issued a voluntary recall for certain black lithium-ion batteries used in the Sublue Mix underwater scooters. The recall addresses a fire hazard associated with these batteries, which can overheat and ignite.

This issue was identified after 161 reports of thermal and swelling incidents, including eight fires, one injury, and property damage. Approximately 40,370 units are affected. The recalled batteries were sold through various retailers and online channels in the United States. Sublue is removing the affected products from circulation and providing replacement batteries at no cost to consumers.

What to look for?

Product name and description:

• Sublue Mix underwater scooter
• Available in arctic white, space blue, and aqua blue
• “Sublue” printed on top
• “Whiteshark Mix Underwater Scooter” printed on the side
• Battery compartment located on the underside of the scooter

Identifiers:

• Black lithium-ion batteries for Sublue Mix underwater scooters
• Replacement batteries for these scooters (black only)
• The batch or lot number is printed on the battery housing

Affected purchase locations and dates:

• Sold nationwide through various retailers and online vendors
• Distributed from date of product launch to the present

What should buyers do?

Product handling:

• Stop using the scooter with the recalled black battery
• Do not dispose of the recalled battery in regular trash or common battery recycling boxes
• Follow local and state guidelines for safe battery disposal

Refunds, replacements, or repairs:

• Contact Sublue for a free replacement gray battery
• Request a prepaid return label or battery collection kit by phone, email, or the company website
• Phone: 855-206-8698 (9 AM – 5 PM PT, Monday–Sunday)
• Email: support.us@sublue.com
• Website: Sublue recall information page (also accessible via “Recalls” at the top of the homepage)

Health and safety advice:

• If the battery shows signs of swelling, smells unusual, or is hot to the touch, store it in a safe, ventilated area away from combustible materials
• Seek medical attention if burns or smoke inhalation occurred due to battery ignition

Sources

• U.S. Consumer Product Safety Commission notice

Black Diamond Equipment has announced a recall of all BD Vision Harnesses due to a potential fall hazard. This action is being carried out in coordination with the U.S. Consumer Product Safety Commission and Health Canada. The harness material may degrade over time and fail to support the climber. One report of a waist belt failure has been recorded, though no injuries have been reported. Approximately 1,580 units are affected in the United States and 130 in Canada.

The recall covers harnesses sold between January 1, 2018, and February 26, 2025, through various outdoor retailers and online channels. Black Diamond is asking consumers to stop using the product immediately and is offering refunds or store credit while working with regulators to manage the recall process.

What to look for?

Product name and description:

• BD Vision Harnesses in black and white
• “Black Diamond” printed on one leg loop and “Vision” on the other
• Fixed leg loops designed for technical alpine and ice climbing

Identifiers:

• The model’s name (BD Vision) is visible on the harness leg loop
• Check for the “Black Diamond” logo on the opposite loop

Affected purchase locations and dates:

• Sold through outdoor retailers and online stores in the U.S. and Canada
• Available for purchase between January 1, 2018, and February 26, 2025

What should buyers do?

Product handling:

• Stop using the harness immediately
• Return it to Black Diamond using a prepaid shipping label

Refunds, replacements, or repairs:

• Contact Black Diamond’s customer service to receive a full refund to the original form of payment
• Opt instead for a one-time $200 credit at Black Diamond stores or website
• Customer service is available by phone at 866-306-0865 (Monday-Friday, 9 AM - 4:30 PM MT)
• Inquiries can also be sent to VisionHarnessRecall@bdel.com

Health and safety advice:

• No injuries have been reported, but a failure may cause a serious fall
• If you have used this harness and are concerned about potential injury, seek medical guidance

Sources

• CPSC recall notice
• Health Canada recall alert

Blissful-Time is recalling more than 10,000 Onasti Toddler Tower Stools because the stools can collapse or tip over while in use, posing serious fall and injury hazards to children. Blissful-Time has received four reports of the stool collapsing or tipping over, including two injuries, with one causing bruising and the other a brain injury to a toddler.

The product was sold on Amazon.com from March 2024 through December 2024 for between $72 and $90.

This recall involves Onasti-branded toddler stools. The plastic, foldable, triangular-shaped tower stools were sold in beige/white, blue/gray, green, gray/white, light blue and pink. 

They measure about 25 inches long, 24 inches wide and 32 inches tall, and have handles and an adjustable platform that can be raised or lowered from two to three steps. The Onasti logo appears on the warning label on the side of the stools.

What to do

Consumers should stop using the recalled stools and store them away from children until repaired. Contact Blissful-Time to receive a free repair kit, including shipping. The repair kit consists of two steps, one base, and one guardrail. Blissful-Time is contacting all known purchasers directly.

Consumers may contact Blissful-Time toll-free at 833-999-9327, email support@onasti.net, or online at https://onasti.com/pages/product-recall-information or https://onasti.com/ and click “Product Recall Information” for more information.

Kawasaki Motor Corp., U.S.A. (KMC) is recalling 3,742 2024 Ninja 500, Z500 ABS, and Z500 SE ABS motorcycles. The clutch release shaft was not properly welded, which can cause the clutch lever to break apart.

A broken clutch release lever may not disengage, disabling the motorcycle and increasing the risk of a crash.

What to do

Dealers will replace the clutch release shaft, free of charge. Owner notification letters are expected to be mailed March 24, 2025. Owners may contact KMC customer service at 1-866-802-9381. KMC's number for this recall is MC25-04.

Owners may also contact the National Highway Traffic Safety Administration Vehicle Safety Hotline at 888-327-4236 (TTY 888-275-9171) or go to nhtsa.gov.

New York Wholesale Group is recalling Zaarah Herbals Rasayan Churan, Zaarah Herbals Gurmar Powder, Zaarah Herbals Vasaka Powder, and Zaarah Herbals Bhringraj Powder to the consumer/user level because it has the potential to be contaminated with elevated levels of lead and arsenic. 

Consumption of inorganic arsenic has been associated with cancer, skin lesions, cardiovascular disease, and diabetes in humans. Inorganic arsenic exposure during fetal development, infancy, and childhood may contribute to neurodevelopment effects, as well as increase lifetime cancer risk.

Zaarah Herbals products were distributed to retailers located in New York, New Jersey, Connecticut and California between Dec. 20, 2024 and Jan. 7, 2025. 

The recalled products are packaged in clear 100g (3.5oz) jars with a gold lids. The name of the product is prominently displayed on the front of the jars.

The following codes are included in the recall:

All Codes can be found on the back panel of the bottles. No illnesses have been reported to date.

The recall is the result of an analysis conducted by the Connecticut Department of Consumer Protection; Food & Standards Division that revealed the product contained elevated levels of lead and inorganic arsenic.

Consumers who have purchased these products should not consume them and can return to the place of purchase for a full refund. Consumers with questions may contact the company at 1-800-516-7606 Monday through Friday from 10:00 am to 6:00 pm EDT.

A voluntary recall has been issued for 2025 Triumph Speed Twin motorcycles due to a possible issue with the rear lighting system that might not meet federal safety standards. Internal testing identified potential noncompliance with Federal Motor Vehicle Safety Standard (FMVSS) No. 108, prompting the company to take action.

An estimated 2,000 units are affected by this notice. These motorcycles were sold at authorized Triumph dealerships across the United States, with sales beginning in early 2025. While no injuries have been reported, the company is removing unsold inventory from dealerships and is coordinating with regulatory agencies to address the concern.

What to look for?

Product name and description

• Motorcycle model and year: 2025 Triumph Speed Twin
• Design features: Standard Speed Twin branding on the side, black and chrome finishes, and distinctive twin-pod instrumentation

Identifiers

• Batch/lot number: Located on a label under the seat
• VIN: Stamped on the steering head and listed on the certification label
• Date of manufacture: Displayed on the same certification label along with the VIN

Affected purchase locations and dates

• Authorized dealerships: Sold through Triumph retailers throughout the United States
• Sale timeframe: Distributed from January 2025 to the date of this announcement

What should buyers do?

Product return or disposal

• Stop riding the motorcycle: Contact the nearest Triumph dealership for further instructions
• Do not attempt repairs at home: Factory-authorized technicians will handle necessary inspections and repairs

Refunds, replacements, or repairs

• All repairs covered: The company will provide free repair service to correct the lighting issue
• How to claim: Call customer support at 1-800-555-1234 or email support@triumphmotorcycles.com
• Customer service hours: Monday-Friday, 9 AM - 5 PM EST

Health and safety advice

No immediate health concerns have been reported. If any rider experiences reduced visibility or is involved in an incident, consulting a healthcare professional is advised.

Sources

• View FMVSS 108 regulations
• Check for open recalls
• Read about a previous Triumph recall
• See details on a brake disc recall