Archive
426 recalls were announced in May 2022.
Of the 426 recalls this month scored against our rubric, 3% are Critical, 16% are Severe.
Which agencies issued them
Carparts.com is recalling specific oil filter housings because a seal defect may cause oil leaks, increasing the risk of fire or engine failure.
Daimler Trucks North America is recalling 2021-2022 FCCC MT50E walk-in vans because a faulty shift knob may cause unintended movement.
Daimler Trucks North America is recalling approximately 17 certain 2022 Freightliner Cascadia trucks because the antilock brakes and electronic stability control can be manually disabled, violating federal safety standards and increasing crash risk. The company will repurchase affected vehicles.
Daimler Trucks is recalling commercial trucks with incorrect weight-rating labels that could allow unsafe overloading. Dealers will replace the labels free of charge.
Shyft Group is recalling 2022 Utilimaster Walk-in vans because tire size and pressure labels may be incorrect, potentially leading to improper tire inflation.
Bowlus is recalling 2022 Endless Highways travel trailers because damaged burner control valves may cause a gas leak, increasing fire risk.
Ford is recalling 2016 Super Duty trucks because dust in the steering wheel clock spring may prevent the driver's air bag from deploying.
Kuntry Kustom RV is recalling 2017-2020 Rich Specialty Trailers because propane regulators may fail, increasing pressure and fire risk.
Ford is recalling 2021 Mustang Mach-E all-wheel drive vehicles because a software error may cause unintended acceleration or loss of power.
Blue Bird is recalling one 2023 Vision transit bus because incorrect software settings allow the engine to start while in gear, increasing crash risk.
Weis Markets is recalling ready-to-eat General Tso Chicken meals sold in seven states because they may contain undeclared milk, a known allergen.
Ford is recalling certain 2022 Mustang vehicles with misaligned front-facing cameras that disable forward collision avoidance and other safety features. Owners should contact Ford customer service at 1-866-436-7332 to schedule free camera realignment.
Plastic Omnium is recalling fuel tank assemblies used in Nissan and Mitsubishi vehicles because the fuel pump may fail, potentially causing an engine stall and increasing crash risk.
Mitsubishi is recalling certain 2022 Outlander vehicles because the seat belt retractor may deactivate prematurely, leaving child restraints unsecured in a crash. About 2,865 vehicles are affected.
Ford is recalling certain 2020 Escape and 2021 Corsair hybrid vehicles due to insufficient welds in the high voltage battery that may fail, causing loss of drive power and increased crash risk.
Driverge is recalling 2020-2021 Ford Transit vehicles because exposed copper in the relay module may cause a short-circuit and fire.
Chrysler is recalling 2022 Jeep Grand Cherokee vehicles because hazard lights may flash when the brake pedal is applied, potentially confusing other drivers.
Chrysler is recalling certain 2022 Jeep Wrangler vehicles with nonfunctional side marker lights. The defect may reduce vehicle visibility to other drivers, increasing the risk of a crash.
Great Dane is recalling 2019 Freedom Platform trailers that may lack rear impact guard certification plates, potentially affecting safety compliance.
Yamaha is recalling about 4,130 Wolverine RMAX off-road side-by-side vehicles due to damaged fuel tanks that can leak fuel, creating fire and explosion risks. No injuries have been reported to date.
A & C Best Food Trading is recalling TOP SAVOR Licorice Flavored Olive products for containing undeclared sulfites. The recalled item was distributed across 12 U.S. states.
A & C Best Food Trading is recalling Wife Plum pickled plums in 500g jars for containing undeclared sulfites and prohibited Amaranth dye. The product poses serious health risks to sulfite-sensitive consumers.
The Salsa Texan tortillas (coconut flour and blended flour varieties) are being recalled for potentially containing undeclared wheat and whey. Products were distributed online and at farmers markets.
Mickey Mouse Hand Sanitizer (ethyl alcohol 68%, 2.11 oz. bottles) is being recalled nationwide by Best Brands Consumer Products, Inc. due to methanol contamination in Lot #20D21 (expiration 06/30/2022).
SML Distribution is recalling 209,450 units of Skippack COVID-19 rapid test kits that were distributed without FDA authorization or clearance. The kits were distributed nationwide across Alabama, Florida, Georgia, Missouri, New York, Texas, and Wyoming.
Whole Foods Market red lentil dal (12 oz) may contain Listeria monocytogenes. The affected product was distributed to nine states. Consumers should not consume the product.
Beta USA is recalling 2022 350, 390, 430, and 500 RR-S motorcycles because an incorrect front brake hose was installed, which may disconnect and cause a loss of braking.
The Mandalorian Hand Sanitizer has been recalled nationwide due to FDA-detected benzene contamination. The recall affects 346,320 bottles with lot number 20E21.
Siemens Healthcare Diagnostics is recalling Atellica IM Enhanced Estradiol (eE2) 500T diagnostic kits that produce falsely elevated test results in plasma specimens, which could lead clinicians to misinterpret patient results.
A software defect in Philips Azurion imaging systems causes the Patient Type to change unexpectedly during study initiation, altering dose control parameters without operator notification.
Hyundai is recalling certain 2022 IONIQ 5 vehicles due to a software error in the Shifter Control Unit that may disengage the parking brake, allowing the vehicle to rollaway and increasing the risk of a crash.
Dr. Reddy's Laboratories is recalling Lansoprazole 30 mg orally disintegrating tablets (Lot T2000645) because they failed dissolution specifications. The tablets may not dissolve properly, affecting medication effectiveness.
A & C Best Food Trading is recalling Olive King Olives (14 oz) because they contain undeclared sulfites. Consumers with sulfite sensitivity should not consume this product.
Viatris Inc. is recalling alprazolam XR 3mg tablets (lot EH8348) distributed nationwide due to failed dissolution testing. Tablets may not dissolve properly, potentially reducing drug effectiveness.
Macleods Pharma USA Inc. is recalling Losartan Potassium 25 mg tablets due to higher-than-acceptable levels of AZIDO impurity from manufacturing deviations. The affected lots were distributed nationwide.
USDA FSIS issued a public health alert for specific Organic Rancher ground beef products due to potential hard plastic contamination. No illnesses have been reported.
Lupin Pharmaceuticals is recalling 1.47 million bottles of Losartan Potassium Tablets due to chemical impurities exceeding acceptable limits. The affected batches were distributed nationwide.
Elegant Foods has recalled 27 cases of Passion Fruit Mango Macarons due to undeclared food color additives including FD&C Blue #1, Blue #2, Red #3, Yellow #5, Yellow #6, and Red #40. The product was distributed in Wisconsin.
McKesson Corporation is recalling 55,440 tubes of Betamethasone Dipropionate Ointment 0.05% (Augmented) nationwide due to manufacturing compliance deviations. The recall stems from the manufacturer's discontinuation of its stability study program.
Lupin Pharmaceuticals recalls Losartan Potassium tablets for CGMP deviations with AZIDO impurity above limits. The recall affects 657,336 bottles distributed nationwide; no illnesses reported.
Lupin Pharmaceuticals is recalling Losartan Potassium and Hydrochlorothiazide tablets distributed nationwide due to elevated AZIDO impurity levels detected during manufacturing quality control.
Siemens Healthcare is recalling all lots of the ADVIA Centaur Enhanced Estradiol diagnostic test because plasma specimens can produce falsely elevated results, potentially leading clinicians to misinterpret patient results.
Arthrex is recalling 300 K-Wire orthopedic devices that do not meet specified length and diameter requirements. Incorrect dimensions may affect surgical function.
An estradiol diagnostic device has been recalled because it produces falsely elevated test results in plasma specimens. These inaccurate results could cause clinicians to misinterpret patient test results.
restor3d Inc. is recalling Evans Wedge Disposable Trials orthopedic surgical instruments because parts were mixed into other lots during relabeling for extended shelf-life. The recall affects devices distributed nationwide across seven states.
Olympus recalls the GF-UC140P-AL5 ultrasonic gastrovideoscope nationwide because it is no longer compatible with the OER-Pro reprocessing system, creating an infection control risk to patients.
BD Synapsys Microbiology Informatics Software version 4.10 overwrites customer-configured antibiotic codes with BD defaults during system updates, affecting data integrity in clinical microbiology reporting.
Acera Surgical Inc is recalling 83 units of the Restrata RWM1-2X2 medical device (Lot Number 51745) due to a misprinted expiration date on the shelf-box packaging distributed nationwide.
restor3d Inc. is recalling 9 units of Evans Wedge Disposable Trials orthopedic surgical instruments because parts from different lots were mixed during a manufacturing rework and relabeling process.
ASO LLC is recalling approximately 73,668 first aid kits sold under Equate, Meijer, and Care Science brands that contain previously recalled acetaminophen. Affected kits were distributed nationwide.
Siemens Atellica IM Enhanced Estradiol test kits can produce falsely elevated results in plasma specimens, potentially leading to misinterpretation of patient hormone measurements. Approximately 2,044 units worldwide are affected.
Blue Bird is recalling 2023 Vision school buses with Allison transmissions because incorrect software allows the engine to start while in gear, increasing crash risk.
Siemens Healthcare is recalling ADVIA Centaur Enhanced Estradiol diagnostic kits because plasma specimens may show falsely elevated results, potentially leading clinicians to misinterpret patient test results.
Elegant Foods is recalling Raspberry Macarons because the product contains undeclared artificial food colorants including FD&C Blue #1, Blue #2, Red #3, Yellow #5, Yellow #6, and Red #40.
Kia Motors America is recalling 2022 EV6 vehicles due to a software error in the Shifter Control Unit that may disengage the parking mechanism, allowing the vehicle to roll away unexpectedly.
Lupin Pharmaceuticals recalls Losartan Potassium and Hydrochlorothiazide tablets nationwide due to manufacturing deviations that resulted in AZIDO impurity levels above acceptable limits.
Macleods Pharma USA is recalling Losartan Potassium 50 mg tablets nationwide due to CGMP deviations with AZIDO impurity levels above acceptable limits. Affected lots: BLI2002A, BLI2004A, and BLI2104B.
Lupin Pharmaceuticals is recalling Losartan Potassium Tablets 100 mg nationwide due to AZIDO impurity levels exceeding acceptable manufacturing limits. Approximately 1,247,067 bottles were affected.
Elegant Foods recalls Door County Cherry Macaron (63 cases, Wisconsin) for undeclared artificial food colorants including FD&C Blue #1, Blue #2, Red #3, Yellow #5, Yellow #6, and Red #40.
McKesson Corporation is recalling Lidocaine Hydrochloride Topical Solution due to manufacturing deviations related to discontinuation of the stability study program. Approximately 81,757 bottles distributed nationwide are affected.
Macleods Pharma is recalling Losartan Potassium Tablets due to CGMP deviations with azido impurity levels exceeding acceptable limits. The recall affects 5.6 million tablets distributed nationwide.
Nova Bus is recalling 2016-2020 LFS and 2013-2022 LFS Artic buses because a text message board duplicates stop and turn signals, increasing crash risk.
Macleods Pharma USA is recalling Losartan Potassium and Hydrochlorothiazide tablets due to manufacturing quality issues with chemical impurity levels above acceptable limits. Affected lots were distributed nationwide in 30-, 90-, and 1000-count bottles.
Macleods Pharma USA Inc is recalling multiple lots of Losartan Potassium and Hydrochlorothiazide tablets (NDC# 33342-052-07, 33342-052-10, 33342-052-44) distributed nationwide due to AZIDO impurity levels exceeding acceptable limits.
McKesson Corporation is recalling Halobetasol Propionate Ointment 0.05% nationwide after the manufacturer discontinued its stability study program, creating CGMP deviations. Over 13,200 tubes distributed in the United States, Guam, and the Northern Mariana Islands are affected.
McKesson Corporation has recalled Lidocaine Prilocaine Cream 2.5%/2.5% because the manufacturer, Teligent Pharma, Inc., discontinued its stability study program, a deviation from manufacturing standards.
Torrent Pharma Inc is recalling 24,888 bottles of Pantoprazole Sodium 20 mg tablets nationwide due to manufacturing defects causing tablets to crack within bottles.
Baxter Healthcare is recalling Flo-Thru Intraluminal Shunts due to potential foreign matter contamination. The recall involves 300 devices distributed in the U.S. and internationally.
Johnson & Johnson Surgical Vision is recalling tray ring covers (Model OM271000) worldwide due to a potential breach in the sterility barrier that could allow contamination.
Siemens Healthcare Diagnostics is recalling Atellica IM Enhanced Estradiol diagnostic test kits (all lots) due to falsely elevated results in plasma specimens. These inaccurate results could lead clinicians to misinterpret patient data.
The FDA is recalling the VELYS Robotic-Assisted Solution Base due to a software defect in version 1.5.1 related to Daylight Saving Time changes. The defect can cause system errors requiring restart, potentially delaying patient treatment.
SCA Pharmaceuticals recalled 120 bags of Norepinephrine 8mg injection nationwide due to Current Good Manufacturing Practice (CGMP) deviations. The voluntary recall was initiated April 25, 2022.
Elegant Foods, LLC is recalling Macaron Variety B due to undeclared food colorants on the label. The product contains six FD&C dyes not listed in the ingredient declaration.
Elegant Foods is recalling Mint Macaron products due to missing label declarations for six artificial food colorings. Consumers should stop consumption and return affected products.
Elegant Foods is recalling eggnog macaron cases because the packaging fails to disclose food color additives including FD&C Blue #1, Blue #2, Red #3, Yellow #5, Yellow #6, and Red #40.
McKesson Corporation is recalling Erythromycin Topical Gel USP 2% due to CGMP deviations. The manufacturer discontinued its stability study program, prompting a nationwide recall of all products within their expiration date.
Lupin Pharmaceuticals is recalling Losartan Potassium and Hydrochlorothiazide 100 mg/25 mg tablets nationwide due to AZIDO impurity levels above acceptable limits. Patients should consult their healthcare provider about their medication.
SCA Pharmaceuticals voluntarily recalled 424 bags of fentanyl and bupivacaine injectable solution due to manufacturing control deviations. The product was distributed nationwide in the United States.
restor3d Inc. is recalling 14 units of its Non-Sterile Double Ended Trial Kit because the product was labeled as Small Footprint when it is actually Medium. The lot was distributed nationwide across seven states.
Elegant Foods is recalling Lemon Macarons (Code 213645A) because the product contains six food color additives that are not declared on the packaging.
Elegant Foods is recalling macarons due to missing declarations of six synthetic food colors on the packaging. Consumers sensitive to food dyes should not consume this product.
Elegant Foods is recalling Holiday Macaron Variety packages due to missing label declarations for six FDA-approved food colorants. Consumers with sensitivities to dyes should not consume these products.
Elegant Foods is recalling Fall Spice Macarons because the packaging does not declare six artificial food colors: FD&C Blue #1, Blue #2, Red #3, Yellow #5, Yellow #6, and Red #40.
Elegant Foods is recalling Lavender Macarons (code 21264A) due to undeclared food colors: FD&C Blue #1, Blue #2, Red #3, Yellow #5, Yellow #6, and Red #40. Affected cases were distributed in Wisconsin.
SCA Pharmaceuticals has recalled Vancomycin HCl 1.5g injection bags due to manufacturing process deviations. The product was distributed nationwide.
Akorn, Inc. is recalling 66,744 bottles of Lidocaine Hydrochloride Oral Topical Solution, USP 2% (Lot #370978) nationwide because the product's viscosity was below the required specification.
Macleods Pharma USA is recalling Losartan Potassium and Hydrochlorothiazide tablets due to AZIDO impurity levels exceeding acceptable manufacturing standards. The prescription blood pressure medication was distributed nationwide.
Jaguar Land Rover is recalling 2022 New Range Rovers because improperly tightened fasteners may cause front crash sensors to malfunction, affecting air bag deployment.
Certain 2022 Rivian R1T vehicles have a malfunctioning occupant classification system that fails to deactivate the front passenger airbag when a child or child seat is present, increasing injury risk during a crash.
Braxton Creek RV is recalling 2022 Free Solo, Bushwhacker, and Bushwhacker Plus travel trailers because cracked LP gas fittings may cause a leak and fire.
Custom Fire is recalling 2021-2022 Spartan emergency vehicles because a rear axle part may fracture, potentially causing the parking brake to engage unexpectedly and increasing crash risk.
Mercedes-Benz is recalling 2006-2012 ML, GL, and R-Class vehicles because moisture in the brake booster can cause corrosion, leading to reduced brake performance or failure.
Winnebago is recalling 2021-2023 Ekko recreational vehicles because quick disconnect fittings in the LP gas system may crack, potentially causing a gas leak that could lead to fire.
Mercedes-Benz is recalling 2021 GLB 250 vehicles because a rear axle sensor linkage may be improperly installed, potentially causing headlight glare that increases crash risk.
Tesla recalls 2020-2021 Model 3 and 2021 Model Y vehicles due to incorrectly installed camera cable terminals that cause swapped camera views, impairing collision detection and automatic emergency braking.
Wayne Farms is recalling approximately 585,030 pounds of ready-to-eat chicken breast fillets that may be undercooked. The products were distributed to restaurants and retail locations in North Carolina, South Carolina, and Virginia.
Olympia Meats is recalling ready-to-eat pork deli meat products because they contain undeclared pistachios, a known allergen.
Pop’s Que and Stew is recalling approximately 12,472 pounds of frozen Brunswick stew products that were produced without federal inspection. The products were distributed to retail locations in Alabama, Georgia, Mississippi, and Tennessee.
Sumitomo is recalling certain Sumitomo and Falken tires because a deformation near the bead could cause separation, increasing the risk of a crash.
Cruiser RV is recalling 2022 Shadow Cruiser trailers because a missing breaker cover exposes studs, creating a risk of electrical arcing, fire, and injury.
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