Recalls in April 2020

Ducati North America is recalling 97 model year 2017 Superleggera motorcycles.

The front brake pads may corrode, potentially causing the front brake pads friction material to detach from the backing plate.

If the front brake pads friction material detaches from the backing plate, the motorcycle may experience increased stopping distance, increasing the risk of a crash.

What to do

Ducati will notify owners, and dealers will replace the front brake pads free of charge.

The recall is expected to begin June 20, 2020.

Owners may contact Ducati customer service at (888) 391-5446. Ducati's number for this recall is SRV-RCL-20-001.

Ximi Vogue of Doral, Fla., is recalling about 160 children’s neck pillows.

Paint on the zippers and zipper pulls contains levels of lead that exceed the federal lead paint ban. Lead is toxic if ingested by young children and can cause adverse health effects.

No incidents or injuries are reported.

This recall involves four models of children’s neck pillows in pink, blue, gray, and green plush fabric. The bar code and Ximi Vogue are printed on a tag sewn into the side of the pillow. The pillow covers have zippers on the back.

The neck pillows, manufactured in China, were sold at Ximi Vogue stores in Miami from November 2019, through February 2020, for about $11.

What to do

Consumers should immediately take the recalled children’s neck pillows away from children and contact Ximi Vogue for a full refund.

Consumers may contact Ximi Vogue toll-free at (855) 946 4002) or by email at admin@ximivogueusa.com for more information.

Navistar is recalling about 130 model year 2019 International WorkStar and International HV vehicles with Meritor MX-14-120 EVO steer axles.

The axles may have insufficient lubrication, which may result in damage to the wheel end bearings.

If the bearings are damaged, the wheel may separate and cause a sudden loss of vehicle control, increasing the risk of crash.

What to do

Navistar will notify owners, and dealers will inspect the steer axle wheel hubs for proper fluid level and repair any damaged wheel end components and spindles -- as necessary -- free of charge.

The recall is expected to begin May 1, 2020.

Owners may contact Navistar customer service at (800) 448-7825. Navistar's number for this recall is 20503.

Condies Foods of Kearns, Utah, is recalling 165 units of roll chicken salad on a croissant and SNDW chicken sandwiches on white.

The products may contain soy, an allergen not declared on the label.

There have been no documented illnesses to date.

The following items, shipped to Coremark Distribution centers and sold in 18 stores throughout Utah, are being recalled:

• Roll chicken salad on croissant single item# 43237 Label UPC: 50777445351
• SNDW chicken sandwich on white single item# 43559 Label UPC: 50777444804

Both items have code dates “USE THRU” 03/6/2020 – 05/6/2020, and “USE THRU” 03/6/2020 05/2/2020.

What to do

Customers who purchased the recalled products should not consume them, but return them to the stores where purchased it.

Consumers with questions may contact the company at (801) 969-1448 ext 108 Monday through Friday from 7:30am – 6:00pm (MST).

GSK Consumer Healthcare is recalling five lots of Benefiber Healthy Shape Prebiotic Fiber Supplement powder and Benefiber Prebiotic Fiber Supplement powder.

The products may be contaminated with pieces of green plastic or shavings from bottle caps.

The firm has received one consumer complaint of a green particle inside a bottle of the product.

The following products, sold by retailers and websites throughout the U.S., from October 28, 2019, through January 21, 2020, are being recalled:

What to do

Customers who purchased the recalled products should stop using them immediately.

Consumers desiring a refund or further information may contact the company at (800) 452-0051, Monday – Friday from 8:00am – 6:00pm (EST).

Leviton Manufacturing of Melville, N.Y., is recalling about 102,000 Leviton 50 ampere, non-NEMA electrical connectors, plugs, receptacles and inlets sold in the U.S., and Canada.

The devices can have mislabeled terminal markings, posing an electrical shock hazard.

The firm has received four reports of mismarked devices, including one report of a consumer who received an electrical shock, and three reports of minor property damage to equipment with which the devices were being used.

This recall involves Leviton 50-ampere, non-NEMA electrical connectors, plugs, receptacles and inlet attachment devices.

The recalled connection devices are used to transmit power to electrical equipment that is not hard-wired to a power source.

Leviton is printed on the devices. Date codes can be found on the back cover of connectors and plugs, the side housing of receptacles and inlets, and on the label of each box.

The recall includes the following model/catalog numbers and date codes:  

Only electrical connectors without a blue dot on the device and packaging are included in this recall.

The devices, manufactured in Mexico, were sold at electrical distributors and online at www.Amazon.com from May 2019, through January 2020, for between $40 and $90.

What to do

Consumers should immediately stop using the recalled devices, disconnect power to them and contact Leviton to arrange for a free replacement device.

Consumers may contact Leviton toll-free at (877) 978-2032 from 8 a.m. to 6 p.m. (ET) Monday through Friday or online at www.Leviton.com and click on “Recall Information” at the bottom of the page for more information.

BioFinest of Lindon, Utah, is recalling about 20 bottles of BioFinest Wintergreen Essential Oil.

The product, which contains methyl salicylate, is not child resistant, posing a risk of poisoning if the contents are swallowed by young children.

No incidents or injuries are reported.

This recall involves 1/3-fl.oz (10 mL) and 3.3-fl. oz (100 mL) amber glass bottles with black caps of BioFinest Wintergreen Essential Oil. The 100 mL bottles include a dropper.

The white label on the bottle displays the BioFinest logo, product name and the volume amount of the bottle. The UPC codes 759578392443 (10 mL) and 759578392436 (100 mL) are printed on the bottle’s label.

The oils, manufactured in Germany, were sold online at Biofinest.com from July 2019, through December 2019, for about $11.

What to do

Consumers should immediately store the product in a safe location out of reach of children. Contact BioFinest for instructions on how to dispose of the product and receive a full refund. Biofinest is contacting all known purchasers directly.

Consumers may contact BioFinest toll-free at (888)-726-5171 from 10 a.m. to 5 p.m. (MT) Monday through Friday, by email at support@biofinest.com, or online at www.biofinest.com for more information.

McLaren Automotive Incorporated is recalling 2,763 model year 2016-2020 720S, model year 2019 Senna, model year 2020 GT, and model year 2017-2019 570GT vehicles.

The Noise, Vibration, and Harshness (NVH) foam pad under the fuel tank may retain moisture and corrode the fuel tank, potentially causing a fuel leak.

A fuel leak in the presence of an ignition source increases the risk of a fire.

What to do

McLaren will notify owners, and dealers will remove the NVH foam pad from the vehicle, and inspect and replace the fuel tank -- as necessary -- on 720S, 570GT, and Senna models. A remedy has not yet been yet finalized for GT models.

The manufacturer has not yet provided a notification schedule.

Owners may contact McLaren customer service at (646) 429-8916.

LUS Distribution of Canada is recalling about 3,100 LUS hair dryers & diffusers sold in the U.S., and Canada.

The hair dryers do not have an immersion protection device, posing an electrocution or shock hazard if the dryer falls into water when plugged in.

No incidents or injuries are reported.

This recall involves the LUS Dryer & Diffuser. The handheld hair dryers were sold in white, in a box that also contains a diffuser.

The hair dryers have the model number HD-LUS01 printed under the back end of the hair dryer.

The logos “LUS Brands” and “Love Ur Curls” are located on either side of the back end of the dryer.

The dryers, manufactured in China, were sold online at www.lusbrands.com from November 2019, through February 2020, for between $125 and $144.

What to do

Consumers should immediately stop using and unplug the hair dryers. LUS is contacting all known purchasers and providing a choice of either a full refund of the purchase price or a $175 store credit.

Consumers may contact LUS at (800)-280-1675, by email at support@lusbrands.ca, or online at www.lusbrands.com and click on ‘Safety and Recall Information’ at the bottom of the page for more information.

Naturo Sciences of Wilmington, Del., is recalling about 1,200 bottles of Eiji Essentials Wintergreen Essential Oil.

The packaging of the product, which contains the substance methyl salicylate, is not child resistant, posing a risk of poisoning if the contents are swallowed by young children.

No incidents or illnesses are reported.

This recall involves Wintergreen Essential Oil in a 5-mL amber glass bottle with a black cap and red and black label.

“Eiji,” “Wintergreen”, “100% Pure Essential Oil,” and the volume amount of the bottle are printed on the label. The Eiji logo is printed in blue and product name in white.

The lot number 6321C is printed on the bottom of the bottle.

The oils, manufactured in the U.S., were sold online at Amazon.com, Walmart.com and Groupon.com from December 2017, through April 2020, for about $7.

What to do

Consumers should immediately store the product in a safe location out of reach of children and contact Naturo Sciences for a refund. The firm is directly notifying all known purchasers about the recall.

Consumers may contact Naturo Sciences toll-free at (800) 656-0273 from 9 a.m. to 5 p.m. PT Monday through Friday, by email at support@naturosciences.com and put “Refund” in the subject line of the e-mail and in the body provide your name, address, and photo of the product, or online at www.naturosciences.com and click on “Naturo Sciences Eiji Wintergreen Oil Recall Alert” at the top of the page for more information.

Altec Industries is recalling 92 model year 2017-2020 ST Spray Trucks.

The battery fuse holder may have been improperly mounted, potentially causing an electrical short circuit.

An electrical short circuit can increase the risk of a fire.

What to do

Altec will notify owners, and dealers will install a new battery fuse holder free of charge.

The recall is expected to begin June 16, 2020.

Owners may contact Altec customer service at (877) 462-5832. Altec's number for this recall is CSN 758.

Amneal Pharmaceuticals of Bridgewater, N.J., is recalling three lots of Nizatidine Oral Solution.

The products may be contaminated with N-Nitrosodimethylamine (NDMA), a probable human carcinogen, above levels established by the FDA.

There are no confirmed reports of adverse events directly related to this recall.

The recalled product is a prescription oral product used for the short-term treatment and maintenance therapy of ulcers and for the treatment of esophagitis and associated heartburn due to gastroesophageal reflux disease

The following product, which was distributed directly to wholesalers who further shipped it to retail pharmacies and consumers nationwide, is being recalled:

What to do

Customers who purchased the recalled product directly from Amneal should stop using it and contact Inmar at (855) 319-4807, Monday – Friday, 8:00 am – 5:00 pm (EST) or by e-mail at DrugSafety@amneal.com for further information.

Forest River is recalling 83 model year 2016 Rockwood Lite RLT2604WS and Flagstaff Lite FLT26RLWS recreational trailers.

Due to insufficient clearance between the front tire and slide out actuator, the tire may contact the slide out bracket and become damaged.

A damaged front tire may fail and cause a loss control of the vehicle, increasing the risk of a crash.

What to do

Forest River will notify owners, and dealers will install a lift kit that will provide the proper clearance between the tire and the slide out bracket. Damaged tires will be replaced. These repairs will be performed free of charge.

The recall is expected to begin May 27, 2020.

Owners may contact Forest River customer service at (574) 642-8943. Forest River's number for this recall is 10D-1159.

Royal International Trading of Brooklyn, N.Y. is recalling packages of Tainy Boctoka Dry Fruits Mix Compot Apple.

The product contains sulfites not declared on the label.

No illnesses or allergic reactions have been reported to date.

The product, which comes in a 17.63-oz (500-g) clear plastic package marked with container code 4705932006197, was distributed nationwide in retail stores and through mail orders.

What to do

Customers who have purchased the recalled product should not consume it, but return itto the place of purchase for a full refund.

Consumers with questions may contact the company at (347) 223-1095.

Ocean Spray Cranberries is recalling a single production lot of 5.5-oz cans of Pink Lite Cranberry Juice Drink.

The product may contain sulfites, a common preservative added to many food products, not declared on the label.

No illnesses have been reported to date.

The recalled product was sold in boxes containing six 5.5-oz cans and has any of the following code information:

• Lot: MH0030LPK4
• Pack Case UPC: 03120003782 4
• Can UPC: 03120003682 7
• GTIN Case 0003120023682 1
• GTIN Case 0003120024682 0
• Best Before Date: 24JAN21
• Dates of Distribution: 21FEB2020 through 16APR20

What to do

Customers who purchased the recalled product should take a picture of the “best before date” code on the bottom of the can and then destroy the product.

The picture should be sent to casupport@oceanspray.com.

Consmers with questions may comtact the company at (800) 662-3263, weekdays 9:00 a.m. – 6:00 p.m.(ET), or a the above email address for a coupon replacement and/or for alternate methods to submitting the picture.

Wyndmere Naturals of New Hope, Minn., is recalling about 2,850 bottles of Wyndmere Birch Sweet Essential Oil and Aches and Pains Synergistic Blend.

The packaging of the product, containing methyl salicylate, is not child resistant as required by law, posing a risk of poisoning if the contents are swallowed by young children.

No incidents or injuries are reported.

This recall involves Birch Sweet Essential Oil in a 10 mL cobalt blue glass bottle with a black cap and a yellow label.

“Wyndmere,” “Birch Sweet,” “Pure Essential Oil,” and UPC code 602444000907 are printed on the label.

The batch number 12717-65 is printed on the bottom of the bottle in yellow ink.

The Aches & Pains Synergistic Blend was sold in a 10 mL cobalt blue glass bottle with a black cap and blue label.

“Wyndmere,” “Aches & Pains,” “Synergistic Blend,” and UPC code 602444010609 are printed on the label.

Batch number 112019-65 is printed on the bottom of the bottle in yellow ink.

The oils, manufactured in the U.S., were sold at grocery stores and online at Amazon.com and wyndmerenaturals.com from January 2020, through March 2020, for between $7 and $12.

What to do

Consumers should immediately store the product in a safe location out of reach of children and contact Wyndmere Naturals for a full refund or a free child resistant replacement cap.

Consumers may contact Wyndmere Naturals at (800) 207-8538 from 8 a.m. to 5 p.m. (CT) Monday through Friday, by email at support@wyndmerenaturals.com and in the body of the email provide your name, address, product name and the date you purchased the product, or online at www.wyndmerenaturals.com and click on “Recall – Important Safety Information” a the top of the page for more information.

TransitWorks is recalling 241 Driverge vehicles based on model year 2019-2020 Ford Transit vans with Freedman Seating Company PT Foldaway and GO-ES 3-point Foldaway seats.

The seat belt retractor block-out zone may have not been set correctly, potentially resulting in a seat belt that may not properly secure the occupant.

An unsecured occupant has an increased risk of injury in a crash.

What to do

TransitWorks will notify owners, and dealers will replace the retractors free of charge.

The manufacturer has not yet provided a notification schedule.

Owners may contact TransitWorks customer service at (855) 337-9543.

Buckhead Meat and Seafood of Houston is recalling a small quantity of frozen flounder stuffed with seafood.

The product contains wheat, soy, milk, fish and eggs, allergens not declared on the label.

No illnesses have been reported to date.

The recalled product, packaged in a brown cardboard box with the product name "FLOUNDER STUFFED W SEAFOOD FRZN," item number 7126763 and pack dates ranging from 03/31/20 to 04/15/20, was sold between April 1, 2020, and April 16, 2020, at various locations across the Harris County, Texas, area.

What to do

Customers with allergies or sensitivities to wheat, soy, milk, fish or eggs who purchased the recalled product should not consume it, but discard it or contact the company to return it for a full refund.

Consumers with questions may contact Cecilia Delgado at (281) 405-3235 from 8:00 a.m. – 5:00 p.m. (CST) Monday through Friday, or by email at Cecilia.Delgado@BuckheadMeat.com.

Avet Pharmaceuticals of East Brunswick, N.J., is recalling 100-count bottles of Tetracycline HCl capsules.

The medication has low out of specification dissolution test results, which results in less tetracycline available in the body to fight infection. This can lead to treatment failures.

The firm has not received any adverse event reports or complaints.

The following products, distributed under the Heritage Pharmaceuticals label, are being recalled:

The recalled products, used for treatment of infections caused by susceptible strains of the designated organisms, including upper and lower respiratory infections, skin and soft tissues infections, infections caused by Rickettsiae, as adjunctive therapy in severe acne, were distributed to wholesalers and distributors throughout the U.S. from between August 2019 – March 2020.

What to do

Avet is notifying its distributors and customers by a separate notification to distributors and through Qualanex and is arranging for the return of all recalled products.

Consumers should contact their doctor for further guidance and potential change of treatment before they stop taking this drug product.

Consumers with questions may contact Qualanex at (888) 424-4341. Monday – Friday, 8:00 am – 5:00 pm, (EST) or by email at recall@qualanex.com.