Archive
744 recalls were announced in December 2025.
Of the 744 recalls this month scored against our rubric, 13% are Critical, 9% are Severe.
Which agencies issued them
Dr. Reddy's Laboratories is recalling 4,800 bottles of Varenicline Tablets, 1mg, after the assay value for the affected lot fell below the specification limit at nine-month stability testing.
Beckman Coulter is recalling 38,225 Access 2 Reaction Vessels because certain lots may have a small protrusion or hair-like deformity that can cause instrument errors and delay patient results.
Chetak New York is recalling Deep-brand frozen surti undhiu mix after the product tested positive for Salmonella. The FDA has classified the action as Class I.
Stryker is recalling 294 MV3 bariatric beds because they and Arise 1000EX mattresses have been sold in close proximity, and the two products have not been tested for compatibility.
Orthofix U.S. is recalling 40,956 CONSTRUX Mini Ti Spacer System units because the labeling contains claims that are not consistently present.
C.R. Bard is recalling 116 BD InLay Optima Ureteral Stent Kits, 8 Fr x 26 cm, because the actual stent size may not match the product label.
Lupin Pharmaceuticals is recalling 52,128 bottles of Sertraline Hydrochloride Tablets, 100 mg, over a defective container in which the seal is not adhering to the bottles.
C.R. Bard is recalling 116 Bard InLay Optima Ureteral Stent Kits, 6 Fr x 14 cm, because the actual stent size may not match the product label.
C.R. Bard is recalling 4,350 BD InLay Optima Ureteral Stent Kits, 4.7 Fr x 26 cm, because the actual stent size may not match the product label.
Stryker is recalling 297 Arise 1000EX mattresses because they and certain MV3 beds have been sold in close proximity, and the two products have not been tested for compatibility.
Winder Laboratories is recalling 3,528 bottles of Morphine Sulfate Oral Solution because the size stated on the carton label did not match the size of the bottle inside.
Orthofix U.S. is recalling 61,977 CONSTRUX Mini PTC Spacer System units because the labeling contains claims that are not consistently present.
Orthofix U.S. is recalling 14,201 Forza Ti Spacer System units because the labeling contains claims that are not consistently present.
Steris is recalling 10 AMSCO 7052HP Washer/Disinfectors because a wire connected to the electrical box may shift out of position, which may result in electrical arcing inside the unit.
Chetak New York is recalling Deep-brand frozen mixed vegetables after the product tested positive for Salmonella. The FDA has classified the action as Class I.
Datascope is recalling 11,470 Cardiosave Hybrid Intra-Aortic Balloon Pump systems to issue an instructions for use addendum revising the preventative maintenance schedule.
GE Medical Systems is recalling 1,818 Senographe Pristina mammography systems because some have a missing or incorrect X-Ray Warning label.
Chetak New York is recalling Deep-brand frozen suran after the product tested positive for Salmonella. The FDA has classified the action as Class I.
Datascope is recalling 47 Cardiosave Rescue Intra-Aortic Balloon Pump systems to issue an instructions for use addendum revising the preventative maintenance schedule.
Chetak New York is recalling Deep-brand frozen baby bhindi after the product tested positive for Salmonella. The FDA has classified the action as Class I.
Toyota is recalling certain 2025-2026 Camry Hybrid and 2026 Corolla Cross Hybrid vehicles because a bolt inside the inverter may not be tightened properly, causing incomplete contact at the terminal.
Gillig is recalling 2025 Low Floor transit buses because wheelchair restraints may fail to lock, posing an injury risk.
Mack Trucks is recalling 2010-2016 Granite trucks because incorrect parts from a previous repair may cause brake overheating, increasing the risk of tire blowouts or fires.
Gillig is recalling 2013 Low Floor transit buses because emergency exit window latches may fail during a crash, increasing injury risk.
La Guadalupana Foods is recalling frozen tamales mislabeled as pork because they contain undeclared milk. The recall covers products shipped to four states.
Ford is recalling 6,819 model year 2026 Super Duty F-250 and F-350 vehicles because the right rear axle shaft may have been improperly heat-treated and may break.
Ford is recalling 2022-2025 E-Transit vehicles because the left rear axle half shaft may disengage, causing loss of drive power or vehicle rollaway.
Suzanna's Kitchen is recalling fully cooked breaded chicken products because they contain soy, a known allergen, that is not declared on the label.
Mercedes-Benz USA is recalling 117 AMG E 53 4MATIC+ Wagon vehicles because the transmission wiring harness may be routed too close to the front driveshaft, which can cause a loss of drive power.
Ford is recalling 2025-2026 Corsair and Escape vehicles because rear seat belt retractors may not be securely fastened, increasing injury risk in crashes.
Mercedes-Benz USA is recalling 82 model year 2025-2026 GLE 350 4MATIC vehicles because center rear seat belts may have been installed without the child seat protection function.
Diamond Coach is recalling 2025 VIP buses because wheelchair restraints may fail to lock, increasing injury risk during transit.
Ford is recalling 272,645 F-150 Lightning, Mustang Mach-E and Maverick vehicles because the integrated park module may fail to lock into park when the driver shifts into park.
Honda is recalling 2016-2020 Acura ILX vehicles because contaminated brake fluid may deform a seal, causing an internal leak and reduced brake function.
Honda is recalling 2025 CR-V Fuel Cell EVs because coolant may leak into the fuel cell stack, causing an internal short circuit and loss of drive power.
About 1,330 Primark Little Bear 2-pack soother clips are being recalled because the wooden button can come off exposing a sharp screw, posing choking and laceration hazards.
About 2,840 VEVOR Garment Steamers are being recalled because they can leak or spit hot water. Reported cap failures resulted in two burn injuries, including a second-degree burn with permanent scarring.
Lippert is recalling Q'Straint QRT-Max wheelchair restraints because the retractors may not lock, preventing proper securing of the wheelchair.
BMW of North America is recalling 36,922 model year 2025-2026 X3 vehicles because unexpected steering wheel rotation may occur while the vehicle is stationary.
About 11,650 Vevor ice crushing machines are being recalled because they can experience a thermal event and ignite. Sanven has received two reports of thermal events, including one fire.
About 2,290 X-Pro Eagle and FRP Sahara 40cc youth ATVs are being recalled because their mechanical suspension fails safety requirements and the handlebars pose a laceration hazard.
General Motors is recalling 1,120 GMC Canyon AT4X AEV vehicles because incorrect sensing and diagnostic module software may cause a second stage passenger air bag deployment when only a first stage is intended.
About 8,960 YCXXKJ baby bath seats are being recalled because they are unstable and can tip over while in use, posing a risk of serious injury or death due to drowning.
About 700 model year 2026 Trek Domane+ and Checkpoint+ electric bicycles are being recalled because the chainring bolts can come loose, causing the chainring to separate from the bike.
About 1,300 SKCAIHT children's mermaid costumes are being recalled because they contain a prohibited phthalate, violating the federal phthalates ban.
About 2,650 Uuoeebb infant walkers are being recalled because they can fit through a standard doorway and fail to stop at the edge of a step, and their leg openings can entrap a child's head.
Africa Imports is recalling Organic Moringa Leaf Powder from lot SO-71449 after the product tested positive for Salmonella. The FDA has classified the action as Class I.
Genepro Protein is recalling 250 bags of Genepro Whey 4th Generation protein because the labeling contains incorrect ingredient information and fails to declare milk as an allergen.
Alanwar Food Corp is recalling Sonex brand aluminum pots after the products were found to contain leachable lead levels of 0.323mg/L. The FDA has classified the action as Class I.
Fresenius Kabi USA is recalling 483 cases of Ivenix LVP Primary Administration Sets after incorrect assembly of a specific lot that the firm states could result in serious patient injury.
Bridgestone is recalling Firestone Destination LE3 tires because a belt edge insert may be out of position, causing tread separation and increasing crash risk.
Lucid is recalling 2026 Gravity vehicles because incorrect seat covers may prevent side air bags from deploying correctly, increasing injury risk.
Get Tested International AB is recalling 40 units of its Urinary Tract Infection Test because the product was distributed without premarket approval or clearance.
Philips North America is recalling the IntelliVue Patient Monitor MX550 over a potential issue where the monitors did not alarm.
Philips North America is recalling the IntelliVue MP80 over a potential issue where the monitors did not alarm.
Avion Pharmaceuticals is recalling 804 bottles of Prenate Chewable after positive test results for soy, which is not listed on the label, and a boron amount stated in mg instead of mcg.
Great Lakes Cheese is recalling 15,490 cases of Italian style shredded cheese blend, sold under eight brands, over potential metal fragments originating in a supplier raw material.
Costco is recalling 142,532 retail units of Kirkland Signature Caesar Salad because the 3 oz sealed packet of Caesar dressing may contain plastic material.
Philips North America is recalling the IntelliVue Patient Monitor MX800 over a potential issue where the monitors did not alarm.
Philips North America is recalling the IntelliVue MP2 over a potential issue where the monitors did not alarm.
Philips North America is recalling the IntelliVue MP50 over a potential issue where the monitors did not alarm.
Illumina is recalling 11,916 NextSeq 550Dx reagent kits because flow cell gaskets have a quality issue that may cause leaks during runs, including possible toxic substance exposure to the user.
Great Lakes Cheese is recalling 4,298 cases of pizza style shredded cheese blend, sold under six brands, over potential metal fragments originating in a supplier raw material.
Enterix is recalling 201,426 InSure ONE Fecal Immunochemical Test kits after the test failed sensitivity testing with one test card lot, which may result in false negative results.
Philips North America is recalling the IntelliVue Multi Measurement Server X2 over a potential issue where the monitors did not alarm.
Medtronic is recalling 6,591 Aurora EV-ICD and Clinical EV-ICD single chamber extravascular defibrillators over the potential for delayed time to high-voltage therapy in a rare sequence of events.
Rong Shing Trading NY is recalling 10 cases of Aojia Dried Red Bayberry because the product contains undeclared sulfites at 7.39mg per serving, and cyclamates.
Philips North America is recalling the IntelliVue MP90 over a potential issue where the monitors did not alarm.
Philips North America is recalling the IntelliVue MP20 over a potential issue where the monitors did not alarm.
Blue Bird is recalling 2025-2027 Vision school buses because a missing support brace may cause the wheelchair lift to fail, increasing injury risk.
Water Pure is recalling 17,612 bottles of My Bladder dietary supplement because the product may be contaminated with E. coli O7:K1 (IAI39/ExPEC) and E. coli 1303.
Blue Bird is recalling 2026-2027 Vision and All American school buses because wheelchair restraints may fail to lock, increasing injury risk.
Pacific Seafood is recalling 15,498 lbs of Raw Blackened Shrimp because the shrimp may contain 3.4mg sulfur dioxide per serving and the label does not declare sulfite.
Philips North America is recalling the IntelliVue Multi-Measurement Module X3 over a potential issue where the monitors did not alarm.
Great Lakes Cheese is recalling 1,850 cases of Good & Gather Mozzarella & Parmesan shredded cheese blend over potential metal fragments originating in a supplier raw material.
Philips North America is recalling the IntelliVue Patient Monitor MX850 over a potential issue where the monitors did not alarm.
Dreyer's Grand Ice Cream is recalling 3,410 cases of Haagen-Dazs mini chocolate dark chocolate ice cream bars over undeclared wheat.
Philips North America is recalling the IntelliVue MP5 over a potential issue where the monitors did not alarm.
Philips North America is recalling the IntelliVue Patient Monitor MX750 over a potential issue where the monitors did not alarm.
Philips North America is recalling the IntelliVue Patient Monitor MX400 over a potential issue where the monitors did not alarm.
Hale inc is recalling 54 bottles of Lotsa Pasta Roasted Garlic Infused Olive Oil over the potential for Clostridium botulinum contamination.
Great Lakes Cheese is recalling 4,131 cases of mozzarella and provolone shredded cheese blend, sold under four brands, over potential metal fragments from a supplier raw material.
Great Lakes Cheese is recalling 235,789 cases of low-moisture part-skim mozzarella shredded cheese, sold under 26 brands, over potential metal fragments from a supplier raw material.
Philips North America is recalling the IntelliVue MP60 over a potential issue where the monitors did not alarm.
Philips North America is recalling the IntelliVue Patient Monitor MX500 over a potential issue where the monitors did not alarm.
Costco is recalling 612 retail units of Kirkland Signature Chicken Sandwich with Caesar Salad because the 3 oz sealed packet of Caesar dressing may contain plastic material.
Philips North America is recalling the IntelliVue MP30 over a potential issue where the monitors did not alarm.
Blonde Beard's is recalling 4,888 8 oz bottles of Dojo Asian Wing Sauce because the product contains undeclared soy.
Philips North America is recalling the IntelliVue MP70 over a potential issue where the monitors did not alarm.
Prime Food Processing is recalling frozen Lava Bun with Green Tea Flavor because the products do not declare milk in the Contains statement or the ingredient statement.
Great Lakes Cheese is recalling 117 cases of Food Club Finely Shredded Pizza Style Four Cheese Blend over potential metal fragments originating in a supplier raw material.
Prime Food Processing is recalling 2,243 cases of frozen Lava Bun with Salted Egg Yolk because the products do not declare milk in the Contains statement or the ingredient statement.
Great Lakes Cheese is recalling 1,900 cases of Happy Farms by Aldi Italian Style shredded cheese blend over potential metal fragments originating in a supplier raw material.
Philips North America is recalling the IntelliVue Patient Monitor MX100 over a potential issue where the monitors did not alarm.
Breckenridge Pharmaceutical is recalling 3,397 bottles of Duloxetine Delayed-Release Capsules, 60 mg, over the presence of N-nitroso-duloxetine above the FDA recommended limit.
Breckenridge Pharmaceutical is recalling 7,389 bottles of Duloxetine Delayed-Release Capsules, 60 mg, over the presence of N-nitroso-duloxetine above the FDA recommended limit.
Volkswagen is recalling 3,138 model year 2025 Tiguan vehicles because a fault in the passenger occupant detection system wiring may deactivate the front passenger air bag when the seat is occupied.
Motor Coach Industries is recalling various transit bus models because the front door lower curb view glazing material is incorrect, which may reduce driver visibility and increase crash risk.
Laiwu Manhing Vegetables Fruits is recalling 245 cartons of irradiated onion granules after foreign objects, described as black plastic planting film, were found in the granulated onion powder.
Philips North America is recalling the IntelliVue Patient Monitor MX600 over a potential issue where the monitors did not alarm.
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