Archive
558 recalls were announced in December 2024.
Of the 558 recalls this month scored against our rubric, 1% are Critical, 13% are Severe.
Which agencies issued them
Micro-X Ltd. is recalling 6 units of the MICRO-X Rover Mobile X-ray System due to environmental operating risks. The system requires strict temperature, humidity, and altitude controls to prevent capacitor malfunction, overheating, and unintended start-up.
SE Grocers and Pics by Price Chopper brand griddle pancakes are being recalled by Treehouse Foods due to potential Listeria monocytogenes contamination. Affected products were distributed nationwide in the USA and Canada.
Treehouse Foods is recalling Signature Select Griddle Pancake Mini packages due to potential Listeria monocytogenes contamination. The recall involves 9,907,389 cases distributed across the United States and Canada.
Treehouse Foods is recalling Nature's Path Organic griddle waffles due to potential Listeria monocytogenes contamination. The affected products were distributed nationwide in the United States and Canada.
Treehouse Foods is recalling approximately 9.9 million cases of organic griddle waffles from multiple brands due to potential Listeria monocytogenes contamination. Consumers should not consume the affected products.
Shimadzu laboratory autosamplers are being recalled due to water intrusion from a dehumidifier that can cause electrical short circuits. Affected units are distributed worldwide, including across the United States.
Baxter Healthcare is recalling MiniCap Extended Life PD Transfer Sets due to an increase in complaints of female connector separation from the transfer set body. Peritoneal dialysis patients should contact their healthcare provider.
Pero Family Farms Squash Sliced Zucchini & Yellow Squash is being recalled due to potential Listeria monocytogenes contamination. Consumers should not consume the product and should discard it or return it to the point of purchase.
Baxter Healthcare is recalling the MiniCap Extended Life PD Transfer Set due to reports of the female connector separating from the transfer set body. The defect may compromise dialysis treatment safety.
Treehouse Foods is recalling certain griddle waffle products due to potential Listeria monocytogenes contamination. Affected products were distributed nationwide in the USA and Canada.
Treehouse Foods is recalling Kodiak Cakes griddle waffles nationwide due to potential Listeria monocytogenes contamination in batch codes starting with 2C.
Treehouse Foods is recalling Nature's Path Organic Griddle Waffles (9,907,389 cases) for potential Listeria monocytogenes contamination. Affected products have batch codes starting with 2C and Best By dates from October 1, 2024 through October 11, 2025.
Treehouse Foods is recalling Trader Joe's Griddle Waffles Pumpkin due to potential Listeria contamination. About 9.9 million cases with batch codes starting with 2C and best-by dates October 1 through October 11, 2025, are affected.
Multiple brands of griddle waffles manufactured by Treehouse Foods are being recalled nationwide due to potential Listeria monocytogenes contamination. Affected products include GOOD & GATHER, H-E-B HIGHER HARVEST, BETTERGOODS, BREAKFAST BEST, and SIMPLE TRUTH brands.
MEDLINE has recalled 360 units of its Neuraxial Kit (Lot 23KLA330) because connectors may not fully open, potentially preventing catheters from being inserted as intended. Healthcare facilities should discontinue use and contact MEDLINE.
Treehouse Foods is recalling approximately 9.9 million cases of Krusteaz griddle waffles and related products due to potential Listeria monocytogenes contamination. Products with batch codes starting with 2C and best-by dates through October 11, 2025 are included.
Treehouse Foods is recalling multiple store-brand frozen waffles nationwide for potential Listeria monocytogenes contamination. The recall affects products with batch codes starting with 2C and best-by dates from October 1, 2024 to October 11, 2025.
Treehouse Foods is recalling SELECTION and COMPLIMENTS brand griddle waffles nationwide due to potential Listeria monocytogenes contamination. Consumers should not consume the affected products.
Boston Scientific recalled 16 units of AMS Artificial Urinary Sphincter Control Pumps due to mislabeled packaging where devices labeled as Pressure Regulating Balloons actually contained Control Pumps.
Karl Storz Endoscopy has recalled 105 surgical instruments with holes in their sterility barriers. The defect may compromise product sterility; affected devices were distributed nationwide and internationally.
Multiple brands of frozen blueberry protein waffles are being recalled due to potential Listeria monocytogenes contamination. Products were distributed nationwide in the USA and Canada.
Multiple MEDLINE procedure kits used for epidural and spinal anesthesia have connectors that may not open fully, preventing proper catheter insertion during medical procedures.
Baxter Healthcare is recalling 1,496 units of MiniCap Extended Life PD Transfer Sets due to reports of female connector separation. The affected lots should not be used until assessed by Baxter.
Treehouse Foods is recalling Simple Truth Griddle Waffle Blueberry products nationwide due to potential Listeria monocytogenes contamination. Consumers should discard affected packages.
Smith & Nephew recalls 1,589 RENASYS EDGE wound therapy pumps due to battery charging failure if not properly maintained. Affected patients may experience treatment interruption.
Treehouse Foods is recalling multiple brands of refrigerated griddle waffles nationwide due to potential Listeria monocytogenes contamination. Affected products have batch codes starting with 2C.
Medline recalls 1,975 NEXUS catheter connectors that may not fully open, preventing proper catheter insertion. Affected units were distributed nationwide and internationally.
Defibtech DDP-100 defibrillation pads distributed in Ireland had authorized labels replaced with unauthorized ones, making expired pads appear fresh. Dried hydrogel on expired pads may fail to deliver adequate energy for cardiac resuscitation.
Baxter Healthcare is recalling its MiniCap Extended Life PD Transfer Set (Part Number T5C4325K) due to increased complaints about the female connector separating from the main body of the device.
Treehouse Foods is recalling H-E-B griddle waffles with blueberry and butter due to potential Listeria monocytogenes contamination. The recall affects approximately 9.9 million cases distributed nationwide.
J.R. Watkins is recalling Cooling Menthol Extra Strength Pain Relief Patches nationwide due to manufacturing practice deviations. The recall affects approximately 7,138 patches from lots JC101, JC102, and JC103.
Unexo Life Sciences Private Limited is voluntarily recalling Parche Leon pain relief patches due to manufacturing practice deviations. No illnesses or injuries have been reported.
Abbott is recalling 130 Merlin@home cardiac transmitters that cannot update software after power interruption during firmware download. Affected devices remain on outdated firmware with no ability to receive future updates.
Water condensation may accumulate under the autosampler's thermal insulation and damage the main board, causing communication errors and delays in laboratory testing. Two Shimadzu models are affected: SIL-40C XR CL and SIL-40C X3 CL.
Neogen Corporation has voluntarily recalled LICEOUT liquid lice treatment due to manufacturing practice violations. The recall affects 8,328 jugs distributed to institutions.
Neogen Corporation voluntarily recalled 5,328 sachets of LICEOUT lice treatment due to manufacturing practice violations. The product was distributed to Bob Barker Company for institutional facilities.
FDA recalls THERA CARE COLD HOT MEDICATED PATCH (menthol 5%) due to manufacturing practice deviations. The voluntary recall affects 279,936 patches distributed nationwide.
Medline is recalling Endo Kit models containing Olympus components with missing sterile and manufacturing lot numbers and expiration dates on packaging. Without this labeling, medical facilities cannot verify product expiration or track inventory.
Zyno Medical LLC is recalling Z-800WF infusion pumps due to incompatibility between WiFi software and the pump's operating software. The affected units were distributed in eight U.S. states.
Cheeky Bonsai Pain Relief Patches (Menthol 10%) are being recalled nationwide due to manufacturing facility compliance deviations. The voluntary recall affects 17,928 patches distributed across the US.
JR Watkins Cooling Pain Relief Patches are being recalled due to manufacturing process deviations identified during production.
THERACARE MAXIMUM STRENGTH PAIN RELIEF PATCH (4% lidocaine) is being recalled nationwide due to manufacturing practice deviations. Unexo Life Sciences, the manufacturer, voluntarily initiated the recall after identifying quality control issues.
Unexo Life Sciences is recalling Absorbine Jr Pain Relieving Knee Patch nationwide due to manufacturing process deviations that do not meet FDA standards. No illnesses or injuries have been reported.
HealthWise Menstrual Pain Relief Patch (Menthol 10%) is recalled due to manufacturing quality deviations. The firm-initiated recall affects 10,368 patches distributed nationwide in the US.
Equate Maximum Strength Lidocaine Pain Relieving Patches (4%) are being recalled due to current Good Manufacturing Practice deviations. Approximately 1.1 million patches were distributed nationwide in the US.
Abbott Medical's Merlin@home transmitter cannot upgrade to current software after power interruptions during prior downloads. This affects remote heart device monitoring systems.
Unexo Life Sciences is voluntarily recalling LILAS Feminine Pain Relief Patch nationwide due to manufacturing practice deviations affecting 363,300 patches.
GE Healthcare is recalling certain Proteus XR/A radiographic systems because steel cables in the Wall Stand component have not been replaced at manufacturer-specified maintenance intervals.
GE Medical Systems is recalling SIGNA PET/MR and DISCOVERY PET/MR imaging systems because gradient coils can produce elevated acoustic noise during scanning under specific conditions.
ABSORBINE jr. Extra Large Back Patch containing 5% menthol is being recalled nationwide due to manufacturing compliance deviations. The Class II recall affects 6,848,820 patches distributed by Absorbine Jr., LLC.
Remote Diagnostic Technologies Ltd. is recalling Tempus LS-Manual Defibrillator Model 00-3020 units distributed in eight U.S. states. The devices were labeled incorrectly during servicing with wrong product name and CAT number.
PACCAR is recalling 2025 Kenworth T880 and other commercial vehicles due to steering arm and tie rod bracket fasteners that may fail, resulting in loss of steering control and increased crash risk.
International is recalling 2025 EMV vehicles because a missing circuit breaker may cause the windshield defrosting system to fail, reducing visibility.
Nova Bus recalled 2022-2024 LFS buses for incorrectly installed wheelchair securement systems. The attachment points may be in wrong locations, preventing proper restraint in crashes.
Pierce is recalling 2023-2024 Velocity, Enforcer, and Quantum fire trucks because front steer axle tires are incompatible with the wheels, increasing crash risk.
USDA FSIS issued a public health alert for frozen pork mortadella illegally imported from Ecuador. Consumers should discard the product as it lacks required inspection marks.
Tesla is recalling 2024 Model X vehicles because flickering parking lights and low beam headlights may fail to sufficiently illuminate the roadway, increasing crash risk.
PACCAR is recalling 2024-2025 Kenworth and Peterbilt commercial trucks with insufficient axle bearing lubrication, which may cause wheel hub overheating and fire or loss of vehicle control.
Looking for a different month? Back to 2024.