Archive
744 recalls were announced in December 2025.
Of the 744 recalls this month scored against our rubric, 14% are Critical, 7% are Severe.
Which agencies issued them
Medtronic MiniMed is recalling 8,251 units of the InPen App for Android because reinstalling the app deletes the notification override permission, so audible and vibratory alerts are not received.
Cepheid is recalling 6,325 Xpert BCR-ABL Ultra kits, catalog GXBCRABL-US-10, because specimens with an elevated white blood cell count above 30,000 cells may cause inaccurate results.
Rocket Medical is recalling 110 Rocket 18Fg Seldinger Catheters with Safety Guard because the instructions and kit labeling contain misleading statements that can lead to improper securing.
Mindray is recalling 906 BeneVision Distributed Monitoring System units because a specific workstation hardware configuration may experience audio playback failure or screen freezing.
AVID Medical is recalling 90 Halyard Major Packs over the potential for an incomplete seal on the header bag.
Somerset Therapeutics is recalling 28,660 vials of Cisatracurium Besylate Injection, 200mg/20mL, after out of specification assay results during long term stability testing.
Novocol Pharmaceutical of Canada is recalling 5,825 units of 3% Polocaine Dental mepivacaine injection over a defective container with cracked or broken cartridges.
Novocol Pharmaceutical of Canada is recalling Mepivacaine HCl 3% injection distributed by Benco Dental over a defective container with cracked or broken cartridges.
DSAART is recalling 29 AART Chin Implants because the products deviated from established specifications and were distributed without the required FDA premarket approvals or clearances.
DSAART is recalling 118 AART Gluteal Implants because the products deviated from established specifications and were distributed without the required FDA premarket approvals or clearances.
Somerset Therapeutics is recalling 71,310 vials of Cisatracurium Besylate Injection, 20 mg/10 mL, after out of specification assay results during long term stability testing.
Novocol Pharmaceutical of Canada is recalling 5,520 cartons of Mepivacaine HCl 3% injection over a defective container with cracked or broken cartridges.
DSAART is recalling 369 AART Silicone Carving Implants because the products deviated from established specifications and were distributed without the required FDA premarket approvals or clearances.
Instrumentation Laboratory is recalling 4,506 units of HemosIL SynthAFax partial thromboplastin time reagent because the recalled lots were manufactured with double the preservative concentration.
Sun Pharma/Taro is recalling 17,664 units of Ciclopirox Shampoo 1% after out of specification impurity and degradation results at the 18-month timepoint.
DSAART is recalling 35 AART Calf Implants because the products deviated from established specifications and were distributed without the required FDA premarket approvals or clearances.
Myofunctional Research Company USA is recalling 436 Myosa for Kids devices because the firm mistakenly distributed the product within the US without FDA premarket clearance or approval.
DSAART is recalling 2 AART Malar Implants because the products deviated from established specifications and were distributed without the required FDA premarket approvals or clearances.
Zimmer Surgical is recalling 498 Zimmer Dermatome AN units because the devices may have a misaligned thickness control bar.
Smith & Nephew is recalling 168 BIOSURE HA Screws, 6mm x 20mm, due to a labeling error on the affected lot.
GE Healthcare is recalling 1,221 ViewPoint 6 systems because the Patient History tab in software versions 6.15.3 and 6.15.4 may not include complete patient medical history information.
DSAART is recalling 41 AART Pectoral Implants because the products deviated from established specifications and were distributed without the required FDA premarket approvals or clearances.
Copan Italia is recalling 122,850 units of 1ml DTT liquid reagent because treatment reagent functionality in respiratory specimens fluidification cannot be guaranteed.
Preferred Pharmaceuticals is recalling 575 blister packs of Ondansetron ODT Tablets, 4mg, after the manufacturer reported that the blister packs are not fully sealed and tablets are falling out.
SeaSpine Orthopedics is recalling 310 NorthStar OCT Navigation items because the surgical technique guide incorrectly identified Medtronic Infinity toolcards as compatible.
Novocol Pharmaceutical of Canada is recalling 1,636 cartons of OraVerse (Phentolamine Mesylate) Injection over a defective container with cracked or broken cartridges.
Copan Italia is recalling 122,850 units of 1ml DTT reagent supplied with a sputum transfer device because treatment reagent functionality in respiratory specimens liquification cannot be guaranteed.
Novocol Pharmaceutical of Canada is recalling 40 cartons of Cook-Waite Carbocaine 3% mepivacaine injection over a defective container with cracked or broken cartridges.
Somerset Therapeutics is recalling 52,340 vials of Cisatracurium Besylate Injection, 10 mg/5 mL, after out of specification assay results during long term stability testing.
Zimmer Surgical is recalling 839 Zimmer Air Dermatomes because the devices may have a misaligned thickness control bar.
Novocol Pharmaceutical of Canada is recalling 12,033 cartons of Lidocaine HCl 2% with Epinephrine 1:100,000 injection over a defective container with cracked or broken cartridges.
Novocol Pharmaceutical of Canada is recalling 18,789 cartons of 2% Xylocaine Dental with Epinephrine over a defective container with cracked or broken cartridges.
Datascope is recalling 47 Cardiosave Rescue units to issue an instructions for use addendum updating the Vibration and Shock Table to reference the correct standards.
Datascope is recalling 11,470 Cardiosave Hybrid units to issue an instructions for use addendum updating the Vibration and Shock Table to reference the correct standards.
Altec is recalling 2022-2023 AA55, AM55, AN46, and AN55 vehicles because a missing check valve may reduce boom insulation, increasing the risk of electric shock.
BMW is recalling one 2025 i4 eDrive40 vehicle because the connection between the positive battery cable and the rear power distributor may become loose.
KTM is recalling certain 2025 390 Adventure R, 390 Adventure X, 390 SMC R and 390 Enduro R motorcycles because engine vibrations may break the side stand spring, letting the stand fall to the ground.
Volvo is recalling certain 2021-2025 vehicles across the XC40, XC60, XC90, S60, S90, V60 and V90 ranges because the rearview camera image may not display when the vehicle is in reverse.
Spartan Fire is recalling certain emergency vehicles because a ladder handle may detach, allowing ground ladders to fall off and creating a road hazard.
Honda is recalling certain 2024-2025 CBR650R motorcycles because engine vibration may damage the turn signal switch wire harness, causing a short circuit and a blown fuse.
Tiffin is recalling certain 2025-2026 Open Trail motorhomes fitted with an optional diesel or propane generator because the wiring harness may contain incorrectly sized wires.
Nissan is recalling 2026 Rogue vehicles with an incorrect-size spare tire that does not match the tire placard information. This may lead to improper tire inflation and increased crash risk.
TICO is recalling 2018-2026 Pro Spotter Tandem tractors because a track rod mounting bracket may crack and break, potentially causing loss of steering control.
Couture Co is recalling four models of Volt e-bike carriers because the latch mechanism may wear excessively and disengage while driving.
Lamborghini is recalling certain 2019-2024 Urus vehicles because a software error may deactivate the rearview camera image, so it does not display.
Mercedes-Benz is recalling certain 2022-2023 EQB vehicles because the high voltage battery may fail internally and lead to a vehicle fire while parked or driving.
Maître Saladier Inc. is recalling approximately 6,000 pounds of Lorraine Quiche products containing pork that were imported into the U.S. without the required reinspection.
Zoox is recalling driverless vehicles with older software that may cross into oncoming traffic at intersections, increasing crash risk.
Olympia Provisions is recalling approximately 1,930 pounds of ready-to-eat holiday kielbasa sausages that may contain metal. The recall covers products sold in California, Oregon, and Washington, as well as nationwide online sales.
Coach and Equipment is recalling 2024-2025 Phoenix transit buses with propane conversion kits because the alternator may damage the fuel line, increasing fire risk.
New Flyer is recalling certain transit buses because the antilock braking and stability control modules may fail without warning lights, increasing crash risk.
Volkswagen is recalling certain 2025 Audi models because the automatic locking retractor may fail to engage when a child seat is installed using the seat belt.
Blue Bird is recalling 2019-2027 Vision and All American electric school buses because a loose 12-volt cable may disconnect, causing loss of electrical systems.
Volkswagen Group of America (Audi) is recalling certain 2019–2026 Audi vehicles due to a software error that may prevent the rearview camera image from displaying. This defect reduces driver visibility behind the vehicle and increases crash risk.
Micro Bird is recalling 2018-2019 and 2024-2026 G5e transit buses because the power steering pump may fail to start or shut down unexpectedly, increasing crash risk.
Micro Bird is recalling 2019 and 2021-2026 G5e school buses because the power steering pump may fail to start or shut down unexpectedly, increasing crash risk.
Porsche is recalling certain 2019-2025 Cayenne, 911, Taycan and Panamera vehicles because the rearview camera image may not display when the vehicle is placed in reverse.
Chrysler is recalling certain 2025 Ram 2500, 3500, 4500 and 5500 trucks because a software error may stop the driver's air bag or seat belt pretensioner deploying in a crash and disable stability control.
Ford is recalling 2022-2024 Maverick Hybrid and 2020 Escape Hybrid vehicles because a software defect may cause the vehicle to shift into neutral unexpectedly, increasing crash risk.
Honda is recalling certain 2025 CB1000SP motorcycles because improperly manufactured pistons and piston rings can lead to rod bearing failure, rear wheel lockup, or oil leaking onto the rear tire.
Hyundai is recalling certain 2022-2024 Tucson vehicles with an optional Mobis tow hitch wiring harness because incorrect installation may allow water into the control module.
Hyundai is recalling specific Mobis tow hitch harnesses because incorrect installation may allow water entry, causing lighting failures or electrical short circuits.
About 400 Pedego Fat Tire Trikes are being recalled because the frame can develop a hairline fracture near a weld. Pedego has received 16 reports of frames breaking, including one leg laceration.
Chrysler is recalling specific Mopar Occupant Restraint Controller Modules because a software error may prevent the driver's air bag or seat belt pretensioner from deploying and disable electronic stability control.
About 1,900 AMP MP2 Smart Fitness Machines are being recalled because the arm does not lock properly. Ten reports include lacerations to the head and bruising.
About 260 Currey & Company Electra chandeliers are being recalled because the component connecting the fixture to the ceiling mount is not threaded properly and the fixture can fall.
About 50,330 jars of Mamisan Pain Relieving Topical Ointment are being recalled because the ointment contains lidocaine and the packaging is not child-resistant.
About 840 bottles of Feel The Beard Minoxidil Beard Growth Oil are being recalled because the product contains minoxidil and the packaging is not child-resistant.
Subaru is recalling certain 2026 Forester vehicles because the rear hatch support bracket may detach without warning, allowing the rear hatch to fall unexpectedly and increase injury risk.
About 80 SereneLife above-ground pools 48 inches and taller, models SLPORND15 and SLPORND18, are being recalled because a compression strap may create a foothold allowing a child to access the pool.
About 13,400 Blue Wave above-ground pools 48 inches and taller are being recalled because the compression strap around the outside of the pool legs may create a foothold for children.
About 2,800 17 Stories Furniture 18-Drawer Dressers are being recalled because they are unstable if not anchored to the wall and violate the mandatory standard required by the STURDY Act.
About 11,200 ANNQUAN power strips are being recalled because they do not contain supplementary overcurrent protection, creating a fire risk if overloaded.
About 12,000 JOKOSIS portable bed rails, model HC0262, are being recalled because users can become entrapped within the rail or between the rail and the mattress.
Altec is recalling certain 2023-2025 Aerial Device and Digger Derrick vehicles because the electronic taillight module harness may have inadequate circuit protection.
Ford is recalling 2025-2026 Mustang Mach E vehicles because a software defect may prevent exterior lights from working, increasing crash risk.
About 16,800 Furnulem 8-Drawer Dressers are being recalled because they are unstable if not anchored to the wall and violate the mandatory standard required by the STURDY Act.
Honda is recalling 2024–2026 CBR600RR motorcycles because the cylinder head may have been improperly manufactured, risking rear wheel lockup and engine fire.
International Motors is recalling 2026 IC Bus CECB vehicles because wheelchair retractors may fail to lock, increasing injury risk during transit.
Ford is recalling 2019 Expedition vehicles previously repaired under recall 20V263 because the 'Transmission Not In Park' warning message and chime are shorter than intended.
Ford is recalling certain 2021-2022 Bronco vehicles previously repaired under recall 23V165, because the rearview camera image may still be displayed after a backing event has ended.
About 650 Schwinn Ovation Bicycle Child Carriers are being recalled because the buckles securing the restraints around the child can release during use, posing a fall hazard.
Ford is recalling certain 2025 and 2026 Maverick vehicles because the instrument panel cover may separate during an airbag deployment, potentially striking occupants and increasing injury risk.
Ford is recalling 2022 Transit vehicles where the rearview camera may display a blank image, increasing the risk of a crash while reversing.
General Motors is recalling 2025–2026 Chevrolet Equinox EV vehicles because the pedestrian alert sound system may not produce sufficient volume change between stopped and low-speed operation, failing to meet federal safety standards.
International Motors is recalling 2026-2027 IC Bus CESB school buses because wheelchair retractors may not lock, increasing injury risk.
About 1,040 TopHomer 8-inch pool drain covers are being recalled because they violate the entrapment protection standards of the Virginia Graeme Baker Pool and Spa Safety Act.
About 4,740 KKL Fabric 9-Drawer Dressers are being recalled because they are unstable if not anchored to the wall and violate the mandatory standard required by the STURDY Act.
About 3,090 Meaicezli Play Purse Sets are being recalled because the toy cell phone contains button cell batteries and the toy tablet a lithium coin battery that children can easily access.
African Food on Wheels is recalling 20 boxes of oven dried fish over Clostridium botulinum in uneviscerated fish. The FDA has classified the action as Class I.
Chetak New York is recalling Deep-brand frozen green channa after the product tested positive for Salmonella. The FDA has classified the action as Class I.
Chetak New York is recalling Deep-brand frozen sliced carrots after the product tested positive for Salmonella. The FDA has classified the action as Class I.
Chetak New York is recalling Deep-brand frozen snake gourd after the product tested positive for Salmonella. The FDA has classified the action as Class I.
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.
Moonlight Packing is recalling a further 2,622 cases of loose bulk peppermint peaches over potential Listeria monocytogenes contamination, under enforcement record H-0324-2026.
Chetak New York is recalling Deep-brand frozen punjabi tinda after the product tested positive for Salmonella. The FDA has classified the action as Class I.
Draeger is recalling 14,420 ErgoStar CM 40 airway connectors after multiple complaints in which cracks formed in the hose of specific catheter mounts. The FDA has classified the action as Class I.
Moonlight Packing is recalling 439 bags of 4-count Peppermint Peach packs over potential contamination with Listeria monocytogenes. The FDA has classified the action as Class I.
Draeger is recalling 191,470 ErgoStar CM 45 airway connectors after multiple complaints in which cracks formed in the hose of specific catheter mounts. The FDA has classified the action as Class I.
ByHeart is recalling 3,482,131 cans and 3,531,901 single serve packets of Whole Nutrition Infant Formula after contamination with Clostridium botulinum. The FDA has classified the action as Class I.
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