Archive
666 recalls were announced in February 2022.
Of the 666 recalls this month scored against our rubric, 2% are Critical, 36% are Severe.
Which agencies issued them
Legend Manufacturing is recalling 85 units of 2022 EV and TV trailers because improperly welded couplers may cause the trailer to separate from the tow vehicle.
Proterra is recalling 2017-2022 Catalyst and ZX5 buses because steering gearbox securing bolts may loosen due to insufficient adhesive, risking loss of steering control. Owner notifications were sent October 7, 2022.
Mercedes-Benz is recalling 2022 EQS 450, EQS 580, and AMG EQS 53 vehicles because improperly secured electrical connections may increase the risk of a fire or cause headlight failure.
Tenco Inc. is recalling one 2020 TOR DR-106100 highway carrier because fuel tubes may crack, causing a high-pressure fuel leak that increases fire risk.
SAF-Holland is recalling specific ULX40 trailer axles because insufficient lubrication in the wheel hubs could cause bearing failure and loss of vehicle control.
Ford is recalling 2021 Escape Hybrid vehicles because an incorrectly manufactured engine crankshaft may cause engine damage, leading to stalling or fire.
Temsa is recalling 2020 TS45 motorcoaches because fuel tubes may crack and leak, increasing the risk of a fire.
Nissan is recalling 2022 INFINITI QX60 vehicles because the second-row seat track may be missing a mounting bolt. This could allow the seat track to move during a crash, increasing injury risk.
Certain 2021 Toyota C-HR vehicles have a radar sensor that was not activated during production, disabling the pre-collision system and forward collision avoidance. Dealers will activate the sensor at no cost.
Yamaha is recalling 453 2021 Tracer 9 GT motorcycles because the throttle grip may break if used to lift the bike, potentially causing loss of throttle control and a crash.
Kelly Wynne is recalling about 1,050 Mama & Me MINI children's handbags sold online from July 2020 through October 2021 because metal components contain lead levels that exceed the federal ban. No injuries have been reported.
Revive Rx is recalling HCG 6,000iu injectable medication due to bacterial contamination (Paenibacillus lautus) identified in the product. The affected lot was distributed nationwide.
Tesla is recalling 2021-2022 Model S vehicles due to side curtain air bag inflators that may have been assembled incorrectly. This could cause delayed air bag deployment during a crash, increasing injury risk.
RED MAMMOTH capsules, 400 mg (Lot # DK1027, Exp. 08/01/2023) are being recalled because they contain undeclared sildenafil and tadalafil, making them an unapproved drug marketed without FDA authorization.
Teleflex is recalling Arrow-Trerotola Percutaneous Thrombolytic Device kits worldwide due to reports of tip separation during use, affecting approximately 1,874 units.
Teleflex Medical is recalling Arrow-Trerotola PTD kits due to reports of tip separation during use. The affected device is used for declotting dialysis grafts and fistulae.
CooperSurgical, Inc is recalling 48,645 cartons of Paragard T380A intrauterine contraceptive devices nationwide due to non-sterility concerns. The voluntary recall affects Lot #517001 with expiration date 1/2024.
The FDA is recalling Arrow-Trerotola Percutaneous Thrombolytic Device catheters due to reports of tip separation during use. Approximately 3,668 units were distributed worldwide.
Teleflex recalls approximately 1,400 Arrow-Trerotola Percutaneous Thrombolytic Device (PTD) kits due to reports of tip separation during use. The medical device is used for dialysis graft declotting and has been distributed worldwide.
BASE 10 GENETICS INC is recalling RNAstill Molecular Transport Medium Vials and specimen collection kits nationwide because they lack FDA 510(k) clearance. Approximately 455,791 kits were distributed across 18 states.
STAQ Pharma is recalling a limited number of syringes labeled as Morphine Sulfate PF that actually contain HYDROmorphone HCl PF due to a labeling error. The affected lot was distributed to Colorado, Ohio, and Texas.
MAC DADDY RED Capsules are being recalled because they contain undeclared tadalafil and/or sildenafil without FDA approval. The product was distributed nationwide via Amazon Marketplace.
Arrow-Trerotola Over-The-Wire PTD catheters used in dialysis procedures are being recalled due to reports of tip separation during use. The FDA classified this as a Class I recall affecting 1,265 units worldwide.
Vyaire Medical is recalling 4,189 bellavista 1000 and 1000e ventilators worldwide due to potential cessation of ventilation under specific conditions. This FDA Class I recall poses serious risk to patients who depend on these critical care devices.
Teleflex Medical Inc. is recalling Arrow-Trerotola PTD catheter sets due to reported tip separation during use. The device is used for mechanical declotting of vascular access fistulae and grafts.
McLaren is recalling 2019-2021 GT vehicles because the driver's air bag may be improperly connected, preventing deployment in a crash.
THE RED PILL EXTRA STRENGTH 800 mg capsules are being recalled because they contain undeclared tadalafil, an active ingredient in FDA-approved sexual-enhancement medications. The product was marketed and distributed as an unapproved drug nationwide via Amazon.
ABC Sales 1 Inc is recalling MAC DADDY PURPLE Capsules because they contain undeclared tadalafil and/or sildenafil, active ingredients in FDA-approved prescription drugs, making the product an unapproved drug.
Golden Medal Mushroom Inc is recalling Xuerong brand enoki mushrooms because Listeria monocytogenes was detected in the product. The affected product was distributed in Illinois.
Teleflex Medical is recalling 5,530 Arrow-Trerotola PTD catheter kits due to reports of tip separation during use. The hazard could prevent the device from functioning properly to remove blood clots from dialysis access grafts.
STAQ Pharma is recalling HYDROmorphone HCl PF syringes (lot 21104221A) that were incorrectly labeled as Morphine Sulfate PF. The mislabeling affects approximately 905 syringes distributed in Colorado, Ohio, and Texas.
Je Dois Lavoir LLC is recalling 365 SKINNY High Intensity Capsules (600 mg, 30-count bottles) because the product contains undeclared sibutramine, a drug previously withdrawn from the US market due to safety concerns.
Philips is recalling Zenition 70 wireless foot switches due to a firmware issue that can cause the device to stop responding. This could interrupt imaging procedures if alternative controls are not used.
Pretty Thai Sweet Chili Stir Fry & Barbecue Sauce is being recalled due to potential undeclared peanuts. Consumers with peanut allergies should not consume the product.
Howmedica Osteonics is recalling medical devices because the outer Tyvek lid may separate from the package seal. This affects 32MM -4 V40 TAPER VIT HEAD devices distributed worldwide.
Howmedica Osteonics is recalling Exeter V40 Cemented Hip (125mm) Stem devices due to a potential label mix with 150mm stems. Incorrect labeling could result in wrong implant size being used during surgery.
The FDA has recalled Exeter V40 Cemented Hip (150mm) Stems due to a potential labeling mix-up with the 125mm version. Patients who received the device should verify with their surgeon that the correct size was implanted.
The TJX Companies is recalling about 7,900 Festive Lights Hanukkah Menorahs because the resin and MDF material can burn or catch fire when holding lit candles. Three incidents of burning or catching fire have been reported, with no injuries or property damage.
Bebe au Lait is recalling approximately 8,600 wooden teethers because the string connecting beads can come untied, releasing beads that pose a choking hazard to young children. The company has received six reports of detached beads, including one case where a child placed a bead in their mouth.
Keystone RV recalls 2022 Cougar trailers with incorrectly specified tires. Load Range D tires were installed instead of required Load Range E, creating overload and crash risk.
Envisiontec US Llc recalls FLEXCERA BASE dental resin (574 units manufactured April–September 2021) due to manufacturing in a non-FDA-registered facility and mislabeling of country of origin.
Hill-Rom is recalling 5,470 Liko M220 mobile lifts used in nursing homes due to a missing bushing that can cause wear and potentially lead to patient falls.
Hill-Rom is recalling 1,215 Liko M220 and M230 mobile patient lifts with missing bushings that cause wear and risk of patient falls. Units were distributed worldwide.
Smiths Medical is recalling certain Medfusion syringe infusion pumps due to intermittent alarm system failures that may occur during power-on self-tests outside the warranty period.
Honey Heaven Wholesale Inc is recalling Organic Roasted Salted Cashews because the product contains hazelnuts but is labeled as cashews. Hazelnuts are visible through the package window.
Comoto is recalling specific Bilt motorcycle helmets that may not adequately protect the wearer during a head impact, failing federal safety standards.
Oscor Inc. is recalling 549 units of Destino Twist and Guidestar devices due to potential separation between the threaded hub and cap. Affected devices were distributed in Tennessee, Pennsylvania, and the Czech Republic.
The wireless foot switch in Philips Veradius Unity medical systems can lose function due to a firmware issue. This could cause delays or interruption of medical procedures if alternative input methods are not used.
Olympus OER-Elite Endoscope Reprocessors may have incorrectly assembled detergent and alcohol tank tubing, causing solutions to be dispensed in reversed cycles. This results in ineffective endoscope disinfection and potential patient exposure to residual detergent.
Steamable by Lidl Chopped Spinach is recalled due to possible Listeria monocytogenes contamination. Affected products were distributed to Lidl stores across eight states.
ANI Pharmaceuticals is recalling Alprazolam Tablets USP 0.25 mg nationwide due to current Good Manufacturing Practice (cGMP) deviations. The recall affects multiple lot numbers of 100-count, 500-count, and 1000-count bottles distributed across the United States.
Driscoll's Inc. is recalling fresh strawberries with pesticide residue (Etoxazole) above U.S. limits. Affected products were distributed to California, Oklahoma, Minnesota, Missouri, Maryland, and possibly Ontario, Canada.
Sun Pharmaceutical is recalling Chlorthalidone Tablets USP 25 mg (Lot #P0602, expiration 03/2023) due to stainless steel microscopic wear particles, punch lubricant oil, and silicone particles from the dust cup found in the product.
ANI Pharmaceuticals is voluntarily recalling Alprazolam Tablets USP 0.5 mg in multiple package sizes nationwide due to cGMP (current Good Manufacturing Practice) deviations. The recall affects approximately 205,662 bottles distributed across the United States.
Merete Medical recalled 26 units of Merete PediatrOS RigidTack (pediatric orthopedic implant, 20 mm) due to incorrect marketing label stating 25 mm. Distribution: Illinois and Germany.
Philips is recalling Zenition 50 wireless foot switches (Model #718096) because a firmware issue can cause them to suddenly stop responding, potentially delaying medical procedures.
Lannett Company is recalling Diazepam Oral Solution (Concentrate) 5 mg/mL due to out-of-specification results for related substances, indicating failed impurities and degradation testing.
Audi is recalling 2022 RS 5 vehicles because the B-pillar tire and loading label displays an incorrect maximum weight, which may lead to vehicle overload.
Teligent Pharma is recalling one lot of Erythromycin Topical Gel USP 2% because the product failed to meet specifications for unknown maximum related compounds.
Howmedica is recalling the Dall Miles SM GRIP device because the outer Tyvek protective package may separate from the sealed unit. The affected batch should be inspected before use.
Envisiontec US LLC recalled 795 units of FLEXCERA SMILE dental resins manufactured between April 2021 and September 2021 because they were produced in a non-FDA-registered facility and falsely labeled as German origin.
ANI Pharmaceuticals is recalling Alprazolam Tablets, USP 2.0 mg nationwide due to current good manufacturing practice (cGMP) deviations. The recall affects approximately 70,788 bottles distributed throughout the United States.
Aurobindo Pharma USA Inc. is recalling Moxifloxacin Ophthalmic Solution 0.5% due to failed impurities and degradation specifications. The recall affects 115,776 bottles distributed nationwide.
ANI Pharmaceuticals has recalled Alprazolam Tablets USP 1.0 mg distributed nationwide due to current Good Manufacturing Practice (cGMP) deviations. The recall affects 173,499 bottles across multiple lot numbers.
ANI Pharmaceuticals, Inc. has recalled Pyrazinamide Tablets USP 500 mg due to cGMP (current Good Manufacturing Practice) deviations. The recall affects approximately 5,477 bottles distributed nationwide.
NaturesPlus Advanced Therapeutics Glucosamine Chondroitin MSM Ultra Rx Joint Cream is being recalled due to microbial contamination identified as Pluralibacter gergoviae in a non-sterile product.
A KWIK-STIK quality control kit has an incorrect inner label. The product contains Campylobacter coli, but the inner label states Haemophilus influenzae.
Porsche is recalling 2020-2021 Taycan vehicles with optional rear center seats. The center seat belt buckle wiring harness may obstruct access to child seat anchors, preventing proper installation.
Daimler Trucks North America is recalling 2022 Freightliner Cascadia trucks for a software and brake hardware defect that may cause loss of braking and parking brake functionality, increasing crash risk.
Comoto is recalling Street & Steel Raider motorcycle helmets because they may not adequately protect the wearer in a crash, increasing the risk of injury.
Daimler Vans USA is recalling 2015-2018 Mercedes-Benz Metris vehicles because a defective memory chip may cause the rearview camera image to freeze, increasing crash risk.
Frickenschmidt Foods LLC is recalling ready-to-eat teriyaki beef sticks because they are labeled 'gluten free' but contain wheat. No adverse reactions have been reported.
Joyson is recalling specific curtain air bag inflators because production interruptions may have caused duplicate or missing components, potentially affecting crash performance.
Mercedes-Benz is recalling 2020 GLE 350 vehicles because an unsecured wiring harness may disable power steering, headlights, or wipers, increasing crash risk.
Corfu Foods is recalling 6,570 pounds of frozen swai fillets imported from Vietnam without required reinspection. No illnesses have been reported.
Kia is recalling 2014 Soul vehicles because the front air bags may not deploy in a crash if the control unit loses communication with sensors.
Lance Camper is recalling 2022 1685 and 1985 travel trailers because an improperly secured propane hose may contact leaf springs, causing a gas leak and increasing fire risk.
HME is recalling 2019-2021 AF1 and 1871 vehicles because fuel tubes may crack, causing a high-pressure leak that increases fire risk.
Thor Motor Coach is recalling certain 2020-2021 Omni and Magnitude motorhomes due to incorrectly routed LP gas lines that could damage and cause a gas leak, increasing fire risk.
General Motors is recalling 2021-2022 Chevrolet Corvette vehicles whose rear half-shaft assemblies may be missing ball bearings. This can cause sudden loss of drive power, increasing crash risk.
Continental Tire is recalling certain ContiScoot tires because cracks in the tread grooves can lead to tread separation, increasing the risk of a crash.
Kia is recalling 2013-2014 Optima vehicles previously repaired under recall 20V-100 because a damaged or missing heat-protective tape on the low-pressure fuel hose can cause a fuel leak and increase fire risk.
H&M is recalling about 615 children's sleepwear sets sold online from October to November 2021 because they fail to meet federal flammability standards for children's sleepwear, posing a risk of burn injuries.
Yamaha is recalling approximately 5,000 golf cars and personal transportation vehicles from model years 2021 and 2022 because they can experience brake failure, creating a crash hazard that could cause injury or death.
Ecom Brands has recalled approximately 100,000 BrushX hot air brushes due to lack of immersion protection, creating an electrocution or shock hazard if the device falls into water while plugged in. No injuries have been reported.
Polaris Industries is recalling approximately 7,400 Model Year 2022 MATRYX snowmobiles because the throttle release switch can fail to disengage or the throttle cable can be kinked, posing a crash hazard.
Husqvarna is recalling about 1,400 Automower 435X and 535 all-wheel drive robotic lawnmowers because the lithium-ion battery can overheat and catch fire. The company has received five reports of battery overheating, including two fires.
Lovevery is recalling steel drinking cups with handles included in Inspector Play Kits because the handle can detach, posing a choking hazard to young children. About 169,000 units were sold online from July 2018 through July 2021.
Zeno collapsible infant walkers fail to meet federal safety standards and pose fall and neck entrapment risks to babies. Consumers should stop using the walkers immediately and contact Zeno for a free return and refund.
Brok Products is recalling 8,400 trailer winches because the crank handle may not fit properly, causing the winch to fail under load.
Navistar is recalling 2019 International LT and RH vehicles because the LED backup lights are the wrong color, failing federal safety standards.
Dole Fresh Vegetables is recalling Chopped Fiesta Lime Kit (10.7oz) for potential Listeria monocytogenes. Affected products have lot codes beginning with N or Y and best-if-used-by dates from November 30, 2021 to January 8, 2022.
Dole Fresh Vegetables Inc is recalling two brands of 5oz organic baby romaine clamshells (Naturally Better and Nature's Promise) due to potential Listeria monocytogenes contamination. Products with specific date codes were distributed to 39 states.
Dole Fresh Vegetables Inc is recalling Kroger 10oz Italian Blend vegetables (UPC 011110910455) due to potential Listeria monocytogenes contamination. Affected products with Best if Used By dates between November 30, 2021 and January 8, 2022 were distributed across 38 states.
Dole Fresh Vegetables Inc is recalling Marketside 6oz Baby Greens for potential Listeria monocytogenes contamination. Products were distributed across 36 states with Best if Used By dates from November 30, 2021 to January 8, 2022.
Dole Fresh Vegetables Inc is recalling Kroger 8oz Shredded Romaine (UPC 011110221483) due to potential Listeria monocytogenes contamination. The product was distributed across 36 states.
Dole is recalling Marketside Organic Spinach Arugula Blend due to potential Listeria monocytogenes contamination affecting approximately 2.3 million cases.
Dole, Lidl, and Little Salad Bar chopped salad kits are being recalled due to potential Listeria monocytogenes contamination. Products were distributed to 38 US states.
Morgan Foods is recalling Skyline chili cans that contain undeclared milk, wheat, and soy allergens. The product may actually be cream of chicken soup.
Dole Fresh Vegetables Inc is recalling Kroger 5oz Organic Power Greens due to potential Listeria monocytogenes contamination. The recall affects approximately 2.3 million cases distributed across 43 states.
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