Archive
506 recalls were announced in February 2025.
Of the 506 recalls this month scored against our rubric, 1% are Critical, 25% are Severe.
Which agencies issued them
Volkswagen is recalling certain 2022-2024 Golf GTI vehicles because a software error may delay or deactivate the rearview camera image, failing FMVSS 111.
MicoVention Terumo LVIS stent devices may fail to advance from the introducer due to PTFE material on the stent loop. Eleven units (Lot 0000456768) distributed in China are affected.
The Candy Basket Inc. recalls Lemon Jelly Sticks WHITE because the label fails to disclose Yellow #5 dye and Potassium Sorbate. Consumers with sensitivities to these additives may be at risk.
Cardinal Health is recalling approximately 973,785 Presource Kits due to potential endotoxin contamination in non-sterile surgical strips and patties. The kits were distributed to healthcare facilities worldwide.
The Candy Basket Inc is recalling Raspberry Jelly Sticks DARK for undeclared Red #40 and Potassium Sorbate. A total of 516 four-pound bulk boxes were distributed in California, Oregon, and Washington.
The Candy Basket Inc recalls Marionberry Jelly Sticks DARK due to undeclared food dyes and additives including Red #3, Blue #1, Potassium Sorbate, and Propylene Glycol.
CareFusion 303, Inc. is recalling the BD Pyxis MedStation 4000 medication cabinet due to potential drawer and door failures that could delay access to stored medications.
CareFusion is recalling six models of BD Pyxis medication management systems due to insufficient labeling regarding potential delays in medication access. The manufacturer is strengthening product labeling to address this risk.
Target Corporation recalled Nestle Toll House Valentine's Chocolate Chip cookie dough (UPC 028000344085) due to improper storage temperature. The product was distributed in AK, CA, ID, MT, OR, and WA.
The Candy Basket Inc is recalling Raspberry Jelly Sticks due to undeclared Red #40 and Potassium Sorbate. Products were distributed in California, Oregon, and Washington.
BD Pyxis MedStation Auxiliary ES medication cabinets are being recalled due to potential drawer and door failures following increased complaints. The failures could delay access to medications stored in the cabinet.
The Candy Basket Inc recalls Marionberry Jelly Sticks due to undeclared food additives and dyes. The product was sold in bulk in California, Oregon, and Washington.
Volvo Trucks is recalling certain 2023-2025 New VN trucks because the brakes may take longer than expected to activate, extending stopping distance. This fails FMVSS 121.
Kia is recalling certain 2021-2023 Seltos and Soul vehicles because incorrectly manufactured piston oil rings can result in engine damage, which may cause a stall or a fire.
Thor Motor Coach is recalling certain 2023 Gemini and Compass motorhomes because washers were not installed with the roof mounting brackets, so the solar panel can detach.
Maserati is recalling certain 2021-2025 Grecale, MC20, Granturismo, GranCabrio, Levante, Ghibli and Quattroporte vehicles because radio software may prevent the rearview image displaying.
Nova Bus is recalling 2006-2007 LFS transit buses because they may have an incorrect number of emergency exits, failing federal safety standards.
Volkswagen is recalling certain 2024-2025 Atlas and Atlas Cross Sport vehicles because an engine cover improperly installed after service can come loose, contact hot engine surfaces and melt.
Daimler Vans is recalling certain 2024 Mercedes-Benz eSprinter vehicles because welds on the helical gear within the rear axle drivetrain may fail, causing a loss of drive power.
Ford is recalling certain 2022-2023 Mustang vehicles previously repaired incorrectly under recall 24V-493, because a miscalibrated torque sensor can turn the steering wheel unbidden.
MORryde is recalling IST22-008 suspensions on Grand Design Serenova travel trailers because improperly tightened axle bearing nuts may cause overheating and tire detachment.
Tesla is recalling certain 2023 Model 3 and Model Y vehicles because an overstress condition in the power steering circuit board can cause a loss of power steering assist.
Cybex is recalling certain 2024 travel systems because harness hooks may bend, causing straps to detach and increasing injury risk.
Ford is recalling certain 2022-2024 Maverick vehicles previously repaired incorrectly under recall 23V-848, where the turn signal flash rate does not warn of a failed signal.
Ford is recalling certain 2020-2021 Explorer and Lincoln Aviator vehicles because seat belt buckle anchor bolts at one or more seating positions may be improperly secured.
Ford is recalling certain 2022-2024 Maverick vehicles previously repaired incorrectly under recall 24V-293, where the body control module may deactivate one or both tail lights.
Ford is recalling 2015-2017 Lincoln Navigator vehicles because LED lights on the exterior mirrors may short circuit, increasing the risk of fire.
Setsmart is recalling LoGest Climbing Ropes sold on Amazon from March 2021 through November 2024 because the ropes can weaken and break, creating a fall hazard. One injury from a fall has been reported.
Jaguar Land Rover is recalling 2020 Range Rover Evoque vehicles because the left-side lower knee air bag cover may come loose, potentially preventing proper deployment in a crash.
Igloo is recalling approximately 1.06 million 90-quart rolling coolers because the tow handle can pinch fingertips against the cooler. The company has received 12 reports of fingertip injuries, including amputations and bone fractures.
General Motors is recalling 2025 Chevrolet Express and GMC Savana vans because improper welds on the driver's side door impact beam may reduce occupant protection in a crash.
Terex Advance is recalling 2024 Commander vehicles because an incorrect front axle thrust bearing may cause the axle shaft to break, increasing the risk of a crash.
Umarex USA is recalling about 26,500 T4E TR50 Air Pistols because the CO2 cartridge can eject unintentionally with force. The company has received 30 reports of this occurring, including 7 reports of injury.
Chrysler is recalling specific Mopar Center Stack displays because a transistor may overheat, preventing the rearview camera image from displaying and increasing crash risk.
About 4,400 Spritz Resin Hanukkah Dino Menorahs are recalled due to fire hazard. Target received 58 reports of the resin menorahs catching fire, scorching, charring, or melting when holding lit candles. No injuries reported. Return for full refund.
SHEIN Distribution Corporation recalls about 17,300 children's pajama sets sold on SHEIN.com between August 2023 and November 2024 for violating federal flammability standards for children's sleepwear, which poses a burn injury risk.
Chrysler is recalling certain 2021-2022 Jeep Grand Cherokee and Grand Cherokee L vehicles because a transistor in the centre stack display may overheat and blank the rearview image.
Jaguar Land Rover is recalling 2020 Range Rover Evoque vehicles because the right-side lower knee air bag cover may come loose, potentially preventing proper deployment in a crash.
Rivian is recalling certain 2025 R1S and R1T vehicles because the headlight low beams may fail to illuminate when starting the vehicle in cold weather, failing FMVSS 108.
The 6-in-1 Pounding Game, sold on Temu.com, is recalled because a magnet in the wooden bird can break off and become an ingestion hazard for children.
Toyota is recalling certain 2021-2025 Sienna Hybrid vehicles because the bolts for the third-row seatbacks may not be tightened properly. 167,802 units are affected.
AFTCO is recalling about 820 Youth Solitude Jackets due to a strangulation hazard from the retractable drawstring in the hood. The drawstring can get caught on objects, posing a risk of serious injury or death to children.
BlockBlueLight Multi-Mode Sleep Lamps are recalled because the lithium-ion battery can overheat while charging, creating fire and burn hazards. No injuries have been reported.
Bazzini LLC is recalling NuGo Dark Pretzel/Chocolate Chip Multipack bars due to undeclared milk. The product poses a risk to consumers with milk allergies.
Par Pharmaceutical is recalling Adrenalin Chloride Solution (Epinephrine Nasal Solution) due to a misleading label that resembles the FDA-approved Adrenalin epinephrine injection product, creating potential confusion.
Cairo Bakery Pita Pocket Bread is recalled for containing undeclared milk. Packages with code 01/18 distributed in California may be affected.
Bazzini LLC is recalling NuGo Dark Chocolate Chip bars because they contain undeclared milk, which poses a health risk to consumers with milk allergies.
COREPACK MANUFACTURING INC is recalling White Maeng da kratom powder due to possible Salmonella contamination. The affected product was distributed throughout the United States.
Mutual Trading Company is recalling ANKIMOBO brand prepared monkfish liver (UPC: 72546611224) because the product contains an undeclared milk allergen. The product poses a risk to consumers with milk allergies.
Atkinson Milling Company is recalling Atkinson's Hushpuppies with Onions due to undeclared milk. The product was not labeled as containing milk, posing a risk to consumers with milk allergies.
La Fiesta Food Products is recalling seasoned bread crumbs because they contain undeclared sesame, an allergen not listed on the label. The product was distributed nationwide.
La Fiesta PAN RAYADO Bread Crumbs are being recalled for undeclared sesame, an allergen not listed on the label. The recall affects 2,200 cases distributed nationwide.
The FDA recalled Ivenix Infusion System software versions 5.9.2 and earlier for potential device malfunctions that could affect medication delivery. Two known anomalies may cause pump failure or improper infusion rates.
Bazzini LLC is recalling NuGo Dark Chocolate Pretzel bars because they contain undeclared milk. Consumers with milk allergies should not consume the affected product.
414 newborn resuscitator kits (ROi CPS LLC) recalled for a potential spring defect in the Inline Controller that could prevent proper ventilation pressure in labor and delivery settings.
VidaSlim dietary supplements and beverages are being recalled due to toxic yellow oleander contamination. The FDA Class I recall affects 760 units distributed nationwide.
Atkinson Milling Company is recalling Atkinson's No Onions Plain Hushpuppies due to undeclared milk on the label. Consumers with milk allergies who consume this product risk allergic reaction.
Terberg Benschop is recalling 2023-2024 YT Series vehicles because a steering arm bolt may be improperly tightened, risking loss of steering and a crash.
Common Sense Soap is recalling approximately 33,899 pounds of beef tallow products produced without federal inspection. The products were shipped nationwide and lack a USDA mark of inspection.
FGF, LLC is recalling flavored sour cream cake donuts nationwide due to potential Listeria monocytogenes contamination. Approximately 2.0 million cases distributed in the US and Canada are affected.
Oxoid Limited is recalling 1,406 units of Lev5 Levofloxacin susceptibility discs because packaging may contain Norfloxacin discs instead, which could affect laboratory test results.
FGF, LLC is recalling 2,017,614 cases of yeast ring donuts nationwide due to potential Listeria monocytogenes contamination. The affected product was produced on or before December 13, 2024.
FGF, LLC is recalling over 2 million cases of yeast ring donuts distributed nationwide and in Canada due to potential Listeria monocytogenes contamination. Consumers should not consume the product.
Philips is recalling AD7 and AD7X patient tables from Allura and Azurion fluoroscopy systems. During manual repositioning, fingers can become trapped between the guiding rails and tabletop, potentially causing injury.
Philips has recalled the AD7 and AD7X patient tables used in medical imaging systems because fingers can become entrapped between the tabletop and guiding rails during manual repositioning, potentially causing injury.
Philips is recalling Azurion 7 M12 and Allura patient tables used in medical imaging systems due to a finger entrapment hazard during manual repositioning. Operators and service personnel may suffer finger injury if fingers are caught between the tabletop and guiding rails.
Teva Pharmaceuticals is recalling Granix injection due to failed stability test results showing one peptide did not meet specification limits.
The FDA is recalling Potassium Chloride Extended-Release Tablets (10 mEq) distributed nationwide because they failed dissolution tests. This could affect how the medication is released in the body.
LivaNova's SenTiva VNS generators (48 units) may stop delivering stimulation due to a mechanical defect. Patients may experience return to baseline seizure or depressive symptoms and may require replacement surgery.
Philips IntelliVue Patient Monitor MX550 units may fail to generate an alarm when a Hamilton ventilator is disconnected, creating a patient safety risk. The monitor could remain silent without alerting clinical staff.
Philips Azurion 5 M12 patient imaging systems pose a finger entrapment hazard during manual tabletop repositioning. Operators and service personnel risk finger injury from the longitudinal guiding rails.
FGF, LLC is recalling 2,017,614 cases of frozen chocolate hex donuts nationwide due to potential Listeria monocytogenes contamination. Consumers should not eat the affected product.
FGF cake sticks are being recalled nationwide and in Canada due to potential Listeria monocytogenes contamination. Consumers should not eat the product and should return it to retailers.
Philips is recalling AD7 and AD7X patient tables used in Allura and Azurion medical imaging systems due to a finger entrapment hazard during manual repositioning. Operators and service personnel are at risk of finger injury.
FGF, LLC is recalling Just Baked Yeast Shells due to potential Listeria monocytogenes contamination. The recall affects 2,017,614 cases distributed nationwide in the US and Canada.
The Belmont Medical 3-Spike Disposable Set may leak during priming due to a crack in its female quick connector, potentially delaying warmed infusions in hospital settings.
FGF LLC is recalling Persian Donut item 8201808 nationwide due to potential Listeria monocytogenes contamination. Consumers should not consume the product and should discard it or return it to the retailer.
FGF, LLC is recalling chocolate-coated donut rings nationwide due to potential Listeria monocytogenes contamination. Approximately 2,017,614 cases are affected. No illnesses have been reported.
FGF, LLC is recalling Just Baked Apple Cider Cake Rings due to potential Listeria monocytogenes contamination. Approximately 2,017,614 cases were distributed nationwide in the US and Canada.
The Philips AD7 and AD7X patient tables pose a finger entrapment risk during manual repositioning. Operators and service personnel could sustain finger injuries from the gap between the longitudinal guiding rails and tabletop.
Monkey Spit 'Swamp Mop' BBQ Sauce is being recalled because it contains an undeclared soy allergen in a sub-ingredient. The product was distributed through local markets and online sales nationwide.
FGF, LLC is recalling apple fritter donuts nationwide due to potential Listeria monocytogenes contamination. Consumers should not consume affected products.
FGF, LLC is recalling frozen donuts nationwide due to potential contamination with listeria monocytogenes. Affected products were produced on or before December 13, 2024.
GE Medical Systems is recalling Definium 656HD and Discovery XR656HD X-Ray systems due to an Automatic Exposure Control defect that may allow radiation exposure to exceed intended safety limits.
Ethicon is recalling PROLENE polypropylene sutures because some packages have open seals due to a manufacturing defect. Defective seals may allow pathogens to contaminate the sterile sutures, potentially causing infection.
Volkswagen is recalling certain Tiguan, Arteon and Audi Q3 vehicles because a camera control unit error at startup may prevent the rearview image displaying.
Philips IntelliVue Patient Monitor MX450 units may fail to sound an alarm when a Hamilton ventilator becomes disconnected, potentially delaying detection of the disconnection.
FGF, LLC is recalling cheese paczki products nationwide due to potential contamination with listeria monocytogenes. Affected products were produced on or before December 13, 2024.
FGF, LLC is recalling 2,017,614 cases of plain cake donuts distributed nationwide in the US and Canada due to potential contamination with Listeria monocytogenes. No illnesses have been reported.
FGF LLC is recalling Bavarian Bismark pastry item 8201936 due to potential listeria monocytogenes contamination. The recall covers all product within expiration produced on or before December 13, 2024, distributed nationwide in the US and Canada.
Philips is recalling Azurion 7 B20 patient tables due to a finger entrapment hazard between the tabletop and guiding rails during manual repositioning. Operators and service personnel could suffer finger injury.
Philips Azurion patient tables used in medical imaging systems can trap fingers between the tabletop and rails during manual repositioning, potentially causing finger injury to operators and service personnel.
FGF, LLC is recalling BAV CRM BISMARK DONUT frozen donuts nationwide due to potential Listeria monocytogenes contamination. Consumers should not eat the product.
FGF, LLC is recalling 2,017,614 cases of yeast ring donuts distributed nationwide and in Canada due to potential Listeria monocytogenes contamination. Consumers should not consume the product.
Philips Azurion and Allura system patient tables may trap fingers between the guiding rails and tabletop during manual repositioning, risking finger injury to operators and service personnel.
FGF, LLC has recalled Just Baked Yeast Ring products due to potential Listeria monocytogenes contamination. Approximately 2,017,614 cases were distributed nationwide in the United States and Canada.
FGF, LLC is recalling flavored raspberry Bismark pastries over potential contamination with Listeria monocytogenes. The recall affects product produced on or before December 13, 2024.
Monkey Spit Atomic Mop BBQ Sauce contains undeclared milk from butter, posing a risk to consumers with milk allergies. Affected bottles were distributed primarily to local markets and nationwide through online sales.
FGF, LLC is recalling Bavarian Filled Donuts distributed nationwide due to potential listeria monocytogenes contamination. Consumers should not consume this product.
RemedyRepack Inc. is recalling certain Carvedilol 25 mg tablets because testing found N-nitroso Carvedilol Impurity-1 exceeding FDA's acceptable limit due to manufacturing process deviations.
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