Archive
428 recalls were announced in January 2022.
Of the 428 recalls this month scored against our rubric, 1% are Critical, 37% are Severe.
Which agencies issued them
Newmar is recalling 2020-2022 Super Star and Supreme Aire motor homes because a tire valve stem extension may be damaged, causing loss of tire pressure and increasing crash risk.
Mercedes-Benz is recalling 2021 AMG GT Black Series vehicles because an incorrectly sized front wheel speed sensor wiring harness may damage, impairing safety systems and increasing crash risk.
Samsung SDI is recalling specific high voltage battery packs that may fail, causing a sudden loss of drive power and increasing crash risk.
USDA issued a public health alert for Simply Fresh Market chicken salad products due to possible Listeria contamination. No illnesses have been reported.
Forest River is recalling certain 2022 Vengeance Fifth Wheel trailers because the tire pressure labels may display incorrect information for the front tires, which could result in under-inflated tires and increase the risk of a crash.
Grand Design RVs (2013-2021) are recalled for an improperly secured 110-volt refrigerator wire that may cause electrical arcing and fire. Dealers will inspect and replace damaged wiring at no cost.
Porsche is recalling 2021-2022 Cayenne vehicles due to potential rear axle misalignment following prior repairs. The defect may cause premature tire wear and increase crash risk.
Johnson Health Tech is recalling about 19,900 Matrix T1 and T3 Series commercial treadmills because the power cord can become loose from the power socket, causing sparking, smoking, melting, and fire. No injuries have been reported.
Grand Design is recalling 2020-2021 Imagine travel trailers with cast aluminum cabinet handles that may have sharp edges. The sharp edges could cut or scrape occupants, and dealers will replace the handles free of charge.
Prevost is recalling certain seat brackets that may not meet strength requirements, increasing injury risk in a crash.
GM recalls certain 2021 Tahoe, Suburban, Yukon, and Escalade vehicles for rear driveshaft assemblies with improperly heat-treated internal components that may fail, causing loss of drive power and increased crash risk.
Chrysler is recalling 2019-2020 RAM 2500-5500 vehicles because wiper arms may loosen, reducing visibility in certain weather conditions.
Tesla is recalling certain 2016-2022 Model S and X, 2017-2022 Model 3, and 2020-2022 Model Y vehicles. The Full Self-Driving (Beta) software rolling stop feature may allow vehicles to pass through all-way stop intersections without stopping, increasing crash risk.
Medtronic is recalling the HawkOne Directional Atherectomy System globally due to reports of tip damage that can detach and cause embolization. The device is used to remove arterial plaque in peripheral blood vessels.
Medtronic is recalling 28,094 units of its HawkOne directional atherectomy system due to reports of catheter tip damage and detachment that can cause blood clots in blood vessels.
D & M Smoked Fish, Inc. is recalling Haifa Smoked Turbot Cold Smoked (8 oz) because it may be contaminated with Listeria monocytogenes. The product was distributed in New York and New Jersey.
Lohxa, LLC is recalling SENNA Syrup (sennosides) 8.8 mg/5 mL unit-dose cups due to microbial contamination of the non-sterile product. The recall affects Lot #AM1115S with expiration date 01/2023, distributed nationwide.
Mylan Pharmaceuticals is recalling approximately 73,175 Semglee (insulin glargine) prefilled pens nationwide because some units have a missing label. Patients should check their pens and contact their pharmacist or doctor if affected.
Pierce Manufacturing is recalling 2015-2021 Enforcer, Quantum, Velocity, and Arrow XT fire trucks because fuel tubes may crack and leak high-pressure fuel, increasing fire risk.
Microbiologics Inc is recalling KWIK-STIK and LYFO DISK microbiological reference products contaminated with Staphylococcus epidermidis. Fifty-nine kits were distributed to multiple U.S. states and countries.
Compass Health Brands is recalling 3,734 Voyager Rollator walkers due to cracking wheel spokes that may cause wheels to separate from the axle, potentially resulting in patient falls and injuries.
Sensis cardiac diagnostic systems used in catheterization and electrophysiology procedures are recalled due to a software error (version VD12A) that can temporarily disable cardiac output measurement. No illnesses have been reported.
Geri-Care Pharmaceuticals is recalling about 800 bottles of over-the-counter acetaminophen and aspirin tablets because the packaging is not child resistant, posing a poisoning risk to young children.
Straumann USA LLC is recalling certain Neodent Easypack dental implant kits due to mislabeling where packaging does not match the implant dimensions inside. Affected units contain 3.5x8mm implants instead of the labeled 3.5x13mm size.
AOSKERA is recalling approximately 1,000 children's nightgowns sold on Amazon.com from October 2020 through May 2021 because they fail to meet federal flammability standards for children's sleepwear, posing a burn injury risk.
Stanley Security Solutions is recalling 11 Senior Living Arial Emergency and Nurse Call Systems because they fail to alarm due to increased memory consumption, potentially preventing nursing staff from responding to resident emergencies.
Ortho-Clinical Diagnostics is recalling VITROS High Sample Diluent A Reagent Pack Lot 2190 because it produces lower than expected TSH test results. The recall affects 1,416 units distributed worldwide.
Draeger Medical recalls 26 Fabius MRI Anesthesia Machines due to incorrectly routed internal oxygen hoses. The misrouting can cause oxygen flow to deviate from set levels, risking inadequate patient oxygenation.
Covidien is recalling 66 SonarMed AirWave Monitor Kits because the alarm may fail to sound and sensors may be incorrectly detected as disconnected, potentially causing the monitor to stop monitoring patients without alerting staff.
Greiner Bio-One is recalling 889,200 blood collection tubes (Lot #B21053QG) due to variation in lithium heparin that may cause blood clotting. The tubes were distributed to ten U.S. states.
Aroma Meats LLC is recalling Nethili Pickle products distributed in Oregon because the label fails to disclose that the product contains anchovy, a common food allergen.
Konica Minolta's ImagePilot versions 1.92 and 1.93 software may provide incorrect measurement calculations if improper power sequences are used with AeroDR or Momentum Panel systems.
Philips North America recalls Cardinal Infant Heel Warmers because labeling was changed without FDA approval. The devices cannot be sold or distributed without new FDA clearance.
Toyota is recalling certain 2021 Venza Hybrid vehicles due to water intrusion in rear turn signal lights, which can cause electrical short circuits and lighting failure, increasing crash risk.
Certain 2019-2021 Audi vehicles are recalled for rear axle misalignment that may cause premature tire wear and increase crash risk. Dealers will inspect and adjust the alignment at no charge, replacing any worn tires as needed.
Straumann USA LLC recalls Neodent Easypack Helix GM Acqua dental implants due to mislabeling. Implants have incorrect dimensions compared to carton labels, which could affect surgical planning and placement.
Eguana Technologies is recalling about 245 Evolve Home Energy Storage Systems because the lithium-ion battery modules can overheat and pose a fire hazard. Consumers should contact the company immediately to schedule a free repair or battery replacement.
Gentueri Inc is recalling 4,150 units of Gentueri Viral Transport Medium (VTM) nationwide due to visual turbidity and discoloration that may compromise diagnostic samples in transit.
Aroma Meats LLC is recalling Curry Leaf Powder (Karevepaku Podi) 1/4 KG packages distributed in Oregon because the product was sourced from an unapproved supplier.
Aroma Meats LLC is recalling Mango Pickle (Fresh Avakai) packaged in 500-gram white plastic pouches distributed in Oregon because the product comes from an unapproved source.
Aroma Meats LLC is recalling Curry Leaf Hot Pickle packaged in white plastic pouches (500 grams) distributed in Oregon because the product was from an unapproved source.
Power Selles Imports is recalling ZOCALO AJI LIMO DRIED CHILI PODS due to the presence of mold on the product. The affected product was distributed across multiple states.
Aroma Meats LLC is recalling Daliya Split Powder (Putnala Podi) distributed in Oregon because the product was sourced from an unapproved supplier. Consumers should not use this product.
Dr. Reddy's Laboratories is recalling QC Quality Choice Fexofenadine HCl 60mg and Pseudoephedrine HCl 120mg Extended-Release Tablets nationwide due to failed dissolution specifications that may reduce the medication's effectiveness.
DeWALT is recalling about 8,500 DWCS600 18-inch corded chain saws because the tool can remain running when the switch is in the off position or turn on unexpectedly when plugged in, posing an injury hazard.
Aroma Meats LLC is recalling Jackfruit Mango Pickle (Fresh Panasapottu) distributed in Oregon because the product was sourced from an unapproved supplier.
Aroma Meats LLC is recalling Ginger Pickle (Fresh Allam Avakai) packaged in 500-gram white plastic pouches distributed in Oregon because the product was from an unapproved source.
Philips North America is recalling 5,164,600 units of Infant Heel Warmers due to labeling changes made after FDA clearance without new approval. The devices cannot be distributed or sold without new FDA 510(k) clearance.
Dr. Reddy's Laboratories is recalling Leader brand 12HR Allergy & Congestion Relief tablets due to failed dissolution specifications. The product may not release its active ingredients properly.
Philips North America recalled approximately 2.5 million Heel Snuggler units because labeling was modified after FDA clearance without obtaining updated regulatory approval.
Family Dollar is recalling about 800 beach lounge chairs that can collapse unexpectedly, risking finger entrapment in metal folding joints. The loungers were sold nationwide from January 2019 through September 2021.
Philips is recalling 2,925,800 Medichoice Infant Heel Warmer units because labeling was modified beyond the scope of FDA clearance. The devices cannot be sold without new 510(k) approval.
Philips is recalling 141,750 Infa-Therm Transport Mattresses because modified labeling does not comply with FDA clearance requirements. The devices cannot be distributed or sold without new FDA clearance.
Luminex Corporation is recalling ARIES HSV 1&2 Assay kits due to a potential leak that may occur inside the ARIES diagnostic instrument. No illnesses or injuries have been reported.
VistaPharm is recalling Clobazam Oral Suspension 2.5 mg/mL due to failed stability specifications. The recall affects 18,456 bottles distributed nationwide.
Aroma Meats LLC is recalling Mango Ginger Pickle (Fresh Mamidi Allam) packaged in 500-gram white plastic pouches because the product was sourced from an unapproved manufacturer. The product was distributed in Oregon.
Ingenus Pharmaceuticals is recalling 45,173 cans of Clobetasol Propionate Foam, 0.05%, nationwide due to Current Good Manufacturing Practice (CGMP) deviations. This is a voluntary, FDA Class II recall.
Aroma Meats LLC is recalling Cilantro Sweet Pickles (Kollimini Sweet) distributed in Oregon because the product was sourced from an unapproved supplier.
Medique Products is recalling Extra Strength Headache tablets nationwide after an FDA inspection found they were not manufactured under Current Good Manufacturing Practices.
Teva Pharmaceuticals is recalling Brinzolamide Ophthalmic Suspension 1% due to defective container caps. The notch in the dropper cap could break off and block dispensing of the medication.
Medique Products is recalling Physicians CARE Extra Strength Pain Reliever tablets nationwide because they were not manufactured under Current Good Manufacturing Practices (CGMP), as determined by an FDA inspection.
Aroma Meats LLC is recalling Pulihora Paste distributed in Oregon because the product was sourced from an unapproved facility. Consumers should not consume the product.
Dr. Reddy's Laboratories is recalling Equate Allergy Relief D Extended-Release Tablets distributed by Walmart nationwide due to failed dissolution specifications. The recall affects 137,856 boxes across multiple lot numbers.
CVS Health Allergy Relief D Extended Release Tablets are being recalled because they failed to meet dissolution specifications. The recall affects 41,784 boxes distributed nationwide.
Dr. Reddy's Laboratories is recalling Fexofenadine HCl 60 mg and Pseudoephedrine HCl 120 mg Extended-Release Tablets because the tablets failed to meet dissolution specifications, which may affect the drug's effectiveness.
Aroma Meats LLC is recalling Fresh Banana Pickle packaged in 500 gm clear plastic pouches because the product was sourced from an unapproved supplier. The product was distributed in Oregon.
Medique Products is recalling Medique Pain-Off tablets nationwide after an FDA inspection found the products were not manufactured under Current Good Manufacturing Practices.
Mayne Pharma is recalling Lexette (halobetasol propionate) Topical Foam 0.05% due to manufacturing defects that cause the product to either not dispense or dispense liquid instead of foam. The recall affects 17,113 canisters distributed nationwide.
Dr. Reddy's Laboratories is recalling Kroger Allergy Relief-D tablets (fexofenadine HCl 60mg/pseudoephedrine HCl 120mg) due to failed dissolution specifications. Approximately 11,064 boxes distributed nationwide are affected.
Dr. Reddy's Laboratories is recalling Rugby brand antihistamine and nasal decongestant tablets nationwide due to failed dissolution specifications. The affected product is NDC 0536-1242-07, Lot #AC2106452F with expiration date 3/31/2023.
Aroma Meats LLC has recalled Fish-Pickle packaged in yellow plastic pouches distributed in Oregon because the specific type of fish used is not declared on the label, contrary to regulatory requirements.
Rite Aid Pharmacy is recalling Allergy & Congestion extended-release tablets because two lots failed to meet dissolution specifications. The affected product was distributed nationwide.
Dr. Reddy's Laboratories is recalling Wal-Fex D Extended Release Tablets nationwide due to failed dissolution specifications. The affected product combines fexofenadine (antihistamine) and pseudoephedrine (decongestant).
Dr. Reddy's Laboratories is recalling Mucus Relief D (Guaifenesin Pseudoephedrine HCl ER Tablets) nationwide due to subpotency. The affected product was distributed to Walgreen Co. stores across the USA.
Forest River is recalling specific 2021-2023 transit buses because a failed relay module can increase the risk of a fire. Dealers will install a wire jumper harness free of charge.
Kia is recalling specific 2017-2019 models because a defect may prevent air bags from deploying in a crash.
Certain 2021 Harley-Davidson motorcycles may not display the speedometer or neutral indicator at startup in freezing temperatures, creating a crash risk. Owners should contact Harley-Davidson for a free software update.
Inland Empire Trailers is recalling 50 units of 2021 trailers because improperly tightened axle spindle nuts may cause overheating and loss of control.
Mitsubishi is recalling certain 2022 Outlander vehicles because the fuel pump may fail due to incorrectly fused internal components. Fuel pump failure can cause engine stall, increasing the risk of a crash.
BMW is recalling 2019-2020 K 1600 GT, GTL, and B motorcycles because a rear suspension link strut may be insufficiently strong, potentially affecting stability and increasing crash risk.
Rosenbauer America is recalling 127 Commander, Warrior, and Avenger vehicles because a rear axle drive pinion may fracture, potentially engaging the parking brake without warning.
Nissan is recalling 2014-2016 Rogue vehicles because water intrusion may corrode an electrical connector, increasing the risk of fire.
Hino is recalling one 2021 NJ8A vehicle because air brake hose fittings may lack required manufacturer markings, potentially increasing crash risk.
Kia is recalling 2020 Cadenza vehicles because rear power windows can operate after the ignition is off, increasing injury risk.
Trails West is recalling 2017-2021 Sierra, Classic, Santa Fe, and Freeride trailers because a propane regulator may fail, increasing fire risk.
Marion Body Works is recalling 2021-2022 Spartan Fire vehicles because a rear axle drive pinion may fracture, potentially engaging the parking brake without warning and increasing crash risk.
Ferrara Fire Apparatus is recalling 2019-2022 Inferno, Cinder, and Igniter vehicles because fuel tubes may crack, causing high-pressure leaks that increase fire risk.
Pacific Trailer is recalling RAM A Frame 2 5/16" couplers because improper welding may cause the trailer to separate from the tow vehicle.
Certain 2021-2022 Heartland Cyclone, Fuel, Gravity, and Road Warrior vehicles with Sailun tires may experience belt separation, risking loss of vehicle control. Dealers will replace affected tires at no cost.
NutraCap Labs LLC is recalling Tailor Made Compounding Clarity Capsule 90ct bottles due to undeclared milk. The product was distributed across 25 states.
NutraCap Labs LLC is recalling Mind Functions Brainology Capsules (132ct bottle) because the product contains undeclared milk, a common allergen.
NutraCap Labs is recalling Dynamik Muscle Warbringer Capsules because the product contains undeclared milk, which poses a risk to consumers with milk allergies.
NutraCap Labs LLC is recalling Huge Nutrition Enhance Capsules 240ct bottles because they contain undeclared milk, which poses a risk to consumers with milk allergies.
NutraCap Labs LLC is recalling TM Nutrition Restoration Pineapple 19oz jars because the product contains undeclared milk, a common allergen. The recall affects 80,169 units distributed across 25 states.
Panda Supps Fierce Panda's Blood (Strawberry) 25oz jars are recalled because they contain undeclared milk. The product was distributed across 25 states.
Vee Tyre is recalling specific Tri-Ace Pioneer A/T III tires because the sidewall may separate, increasing the risk of a crash.
NutraCap Labs LLC is recalling ViVa/ViValife Joint Support Capsules 90ct bottles because the product contains undeclared shellfish, which poses a serious risk to consumers with shellfish allergies.
NutraCap Labs LLC is recalling Enduring Atlas Keto Sleep Capsules (120ct, UPC X001V3J6ZL, Lot #2012314, Exp 12/2022) because the product contains undeclared milk, posing a risk to consumers with milk allergies.
NutraCap Labs LLC is recalling Black Magic AUS Brain Waves Capsules 4 ct sample packs because they contain undeclared milk, a common allergen that may pose a serious health risk to consumers with milk allergies.
NutraCap Labs LLC is recalling DL NutritZone Genone Naturals Joint Support Capsules (150ct) because the product contains undeclared shellfish. The recall affects approximately 80,169 bottles and jars distributed across 25 U.S. states.
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