December 2024 recalls

558 recalls were announced in December 2024.

What the numbers show

Critical: 6
Severe: 68
High: 413
Moderate: 70
Low: 1

Of the 558 recalls this month scored against our rubric, 1% are Critical, 12% are Severe.

Which agencies issued them

501–558 of 558

HighFDA (Food)·F-0156-2025·2024-12-04
Treehouse Foods Griddle Pancakes Recalled for Potential Listeria Contamination
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.
Product
SE GROCERS 12/16.5oz GRDL PNCK HSTYLE-SEGGR UPC 038259117194 PICS BY PRICE CHOPPER 12/16.5oz GRDL PNCK HSTYLE-PRCHP UPC 041735157386
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0192-2025·2024-12-04
Kodiak Cakes Griddle Waffles Recalled for Potential Listeria Contamination
Treehouse Foods is recalling Kodiak Cakes griddle waffles due to potential Listeria monocytogenes contamination. Affected products have batch codes starting with 2C with best by dates from October 1, 2024 to October 11, 2025.
Product
KODIAK CAKES 8/10.72oz GRDL WFL DRKCH REFORM-KDKCS UPC 705599012709
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0210-2025·2024-12-04
Trader Joe's Griddle Waffles Pumpkin Recalled for Listeria Contamination Risk
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.
Product
TRADER JOE'S 24/9.9oz GRDL WFL PMPKN - TRDJO UPC 000000517263
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0185-2025·2024-12-04
Griddle Waffles Recalled for Potential Listeria Contamination
Multiple brands of griddle waffles are being recalled due to potential Listeria monocytogenes contamination. The recall affects products distributed nationwide in the USA and Canada.
Product
SELECTION 1/1.68kg GRDL WFL CHOC CHIP-SLCTN UPC 00059749977692 NO NAME 12/280g GRDL WFL CCH - NNAME UPC 060383987701 SELECTION 12/280g GRDL WFL CCH-SLCTN UPC 059749904711 COMPLIMENTS 12/280g GRDL WFL CHOC CHIP - CMPLM UPC 055742500509 HANNAFORD 8/12.3oz GRDL WFL CHOC CHIP-HANNA U
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0201-2025·2024-12-04
Treehouse Foods Griddle Waffles Recalled for Potential Listeria Monocytogenes
Treehouse Foods is recalling griddle waffles sold under multiple retail brands due to potential Listeria monocytogenes contamination. Approximately 9.9 million cases were distributed nationwide.
Product
HANNAFORD 8/12.3oz GRDL WFL MLTGRN-HANNA UPC 041268196319 FOODHOLD 8/12.3oz GRDL WFL MLTGRN-FDHLD UPC 688267081958 H-E-B 12/12.3oz GRDL WFL MGRN - HEBUT UPC 041220908233 BEST CHOICE 12/12.3oz GRDL WFL MLTGRN-BSTCH UPC 070038622116 HARRIS TEETER 12/12.3oz GRDL WFL MGRN - HARTE UPC
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0063-2025·2024-12-04
Drug recall: Absorbine Jr. Ultra Strength Pain Patch manufacturing deviations
Absorbine Jr. Ultra Strength Pain Patch is being recalled nationwide due to manufacturing process deviations. The voluntary recall affects approximately 4,968,000 patches.
Product
ABSORBINE jr ULTRA STRENGTH PAIN PATCH, Menthol 6.5%, 1 patch per box, Distributed By: Absorbine Jr. LLC, Chattanooga, TN 37402 UPC 8 89476 41318 3, UPC 8 89476 41336 7
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0559-2025·2024-12-04
Baxter MiniCap Peritoneal Dialysis Transfer Set Connector Separation Recall
Baxter is recalling MiniCap Extended Life PD Transfer Sets (Part Number 5C4482) due to reports of the female connector separating from the main body. Approximately 409,464 units are affected worldwide.
Product
Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4482; use in Peritoneal Dialysis
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0530-2025·2024-12-04
AMS Artificial Urinary Sphincter Control Pump: Mislabeled Packaging Recall
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.
Product
AMS Artificial Urinary Sphincter Control Pump
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0537-2025·2024-12-04
Philips dS Breast 16ch 1.5T MRI Recalled for Patient Safety Risk
Philips North America is recalling approximately 5,231 dS Breast 16ch 1.5T MRI systems nationwide due to a potential safety issue that could harm patients during scan preparation or procedures.
Product
dS Breast 16ch 1.5T
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0504-2025·2024-12-04
Defibtech Adult Defibrillation Pads Recalled for Labeling Error Risk
Defibtech is recalling 22,294 DDP-2001 Adult Defibrillation Pads distributed in Ireland. Some pads had unauthorized labels applied, which could allow expired pads to appear current, and dried hydrogel may reduce electrical delivery during use.
Product
Defibtech DDP-2001: Adult Defibrillation Pads For use with AED Models: Lifeline View Auto, lifeline Pro, lifeline ECG, lifeline View (DDU-2XXX Series). -Indicated for use on victims of sudden cardiac arrest (SCA.)
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0531-2025·2024-12-04
AMS Artificial Urinary Sphincter Balloon Mislabeled With Wrong Component
Boston Scientific recalls 52 mislabeled AMS Artificial Urinary Sphincter balloons that may contain a Control Pump instead of the labeled Pressure Regulating Balloon component.
Product
AMS Artificial Urinary Sphincter Pressure Regulating Balloon 61-70 cm H2O
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0544-2025·2024-12-04
Philips Mammotrak Interventional Coil MRI Device Recalled for Patient Safety
Philips recalls 5,231 Mammotrak Interventional Coil 3.0T MRI devices nationwide due to a potential safety issue that could harm patients during scan preparation or imaging.
Product
Mammotrak Interventional Coil 3.0T
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0541-2025·2024-12-04
Mammotrak Diagnostic Coil 1.5T Recalled Due to Patient Safety Concern
Philips is recalling 5,231 Mammotrak Diagnostic Coil 1.5T units nationwide because of a potential patient safety issue during MRI scans. The FDA has classified this as a Class II recall.
Product
Mammotrak Diagnostic Coil 1.5T
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0532-2025·2024-12-04
Medline Surgical Kits Recalled for Incorrect Needle and Suture Specifications
Medline Industries is recalling 408 surgical kits from Alabama, Georgia, Massachusetts, New Jersey, and Pennsylvania. Some suture packages within the kits contain incorrect needle types and sizes, and incorrect suture diameters and lengths.
Product
(1) Medline Open Heart CDS, REF CDS840132O, packaged 1 kit/case, non-sterile; and (2) Medline Dr. Davies CV, REF DYNJ903016G, packaged 1 kit/case, non-sterile.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0569-2025·2024-12-04
Baxter MiniCap Extended Life PD Transfer Set—Connector Separation Recall
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.
Product
Baxter MiniCap Extended Life PD Transfer Set (short) with Titanium Spike, Part Number T5C4326K; use in Peritoneal Dialysis
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0540-2025·2024-12-04
Philips dS Breast 7ch 3.0T MRI Coil Recalled for Patient Safety Hazard
Philips is recalling 5,231 dS Breast 7ch 3.0T breast MRI coils distributed nationwide due to a potential safety issue that may harm patients during scan preparation or scanning. The FDA classified this as Class II.
Product
dS Breast 7ch 3.0T
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0159-2025·2024-12-04
Treehouse Foods Griddle Pancakes Recalled for Listeria Risk
Treehouse Foods is recalling H-E-B and Trader Joe's griddle pancake products nationwide due to potential Listeria monocytogenes contamination. Affected products have batch codes starting with 2C and best-by dates from October 2024 through October 2025.
Product
H-E-B 12/14.1oz GRDL PNCK MINI HSTYLE ORG-HEBUT UPC 041220982714 TRADER JOE'S 16/11.3oz GRDL PNCK MINI HSTYLE ORG-TRDJO UPC 686151803778
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0172-2025·2024-12-04
Krusteaz Griddle Waffles Recalled for Potential Listeria Contamination
Treehouse Foods is recalling Krusteaz 12-pack griddle waffles nationwide due to potential Listeria monocytogenes contamination. Affected products have batch codes starting with 2C and best-by dates from October 1, 2024 to October 11, 2025.
Product
KRUSTEAZ 12/9oz GRDL WFL BLBRY MINI-KRSTZ UPC 041820819120
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0167-2025·2024-12-04
Gordon Food Service Waffle Mix Recalled Due to Potential Listeria Contamination
Treehouse Foods is recalling 9.9 million cases of Gordon Food Service waffle mix due to potential Listeria monocytogenes contamination. Affected products have batch codes starting with 2C and best-by dates from October 2024 to October 2025.
Product
GORDON FOOD SERVICE 1/10.8lb GRDL WFL BLGN BFFT - GDNFS
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0169-2025·2024-12-04
Kodiak Cakes Griddle Waffles Recalled Due to Listeria Risk
Treehouse Foods recalls Kodiak Cakes 8/14.8oz Griddle Waffles due to potential Listeria monocytogenes contamination. Affected products carry batch codes starting with 2C and best-by dates from October 1, 2024 to October 11, 2025.
Product
KODIAK CAKES 8/14.8oz GRDL WFL BLGN BLBRY-KDKCS UPC 705599014826
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0560-2025·2024-12-04
Baxter MiniCap Peritoneal Dialysis Transfer Set Connector Separation Recall
Baxter is recalling 22,392 units of MiniCap Extended Life PD Transfer Sets (Part Number 5C4482EJ) due to reports of female connector separation. Affected units were distributed worldwide.
Product
Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4482EJ; use in Peritoneal Dialysis
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0542-2025·2024-12-04
Mammotrak Interventional Coil 1.5T recalled for patient safety risk
Philips is recalling 5,231 units of the Mammotrak Interventional Coil 1.5T nationwide due to a potential safety issue that may harm patients during MRI preparation or scanning.
Product
Mammotrak Interventional Coil 1.5T
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0562-2025·2024-12-04
Baxter MiniCap Peritoneal Dialysis Sets Recalled for Connector Separation
Baxter Healthcare is recalling MiniCap Extended Life PD Transfer Sets due to increasing reports of the female connector separating from the main body. The defect affects 62,718 units distributed worldwide.
Product
Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4483; use in Peritoneal Dialysis
Category
Medical Device
Distribution
0 states
HighFDA (Food)·F-0207-2025·2024-12-04
Kodiak Cakes Mini Griddle Waffles Recalled for Listeria Contamination Risk
Treehouse Foods recalls Kodiak Cakes 8/9.88oz Mini Griddle Waffles sold nationwide due to potential Listeria monocytogenes contamination. Affected products have batch codes starting with 2C and Best By dates from October 1, 2024 through October 11, 2025.
Product
KODIAK CAKES 8/9.88oz GRDL WFL ORIG MINI-KDKCS UPC 705599017148
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0147-2025·2024-12-04
Hannaford Seafood Salad Recalled for Undeclared Soy Protein Allergen
Hannaford brand seafood salad is recalled because it contains undeclared hydrolyzed soy protein. Consumers with soy allergies should be aware of this risk.
Product
Hannaford brand seafood salad; Net Wt. 12 oz. (340g); INGREDIENTS: SEAFOOD BLEND (FISH PROTEIN [ALASKA POLLOCK AND/OR PACIFIC WHITING], WATER, WHEAT STARCH, SUGAR, SORBITOL, MODIFIED POTATO STARCH, CONTAINS 2% OR LESS OF: NATURAL AND ARTIFICIAL CRAB FLAVORS [SWIMMING CRAB, SNOW C
Category
Food
Distribution
5 states
HighFDA (Devices)·Z-0538-2025·2024-12-04
Philips dS Breast MRI System Recalled for Patient Safety Hazard
Philips dS Breast 16ch 3.0T MRI systems are being recalled due to a potential safety issue that could harm patients during medical scans. The FDA-mandated Class II recall affects 5,231 units distributed nationwide.
Product
dS Breast 16ch 3.0T
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0154-2025·2024-12-04
Breakfast Best Griddle Pancakes Recalled for Potential Listeria Contamination
Treehouse Foods is recalling Breakfast Best griddle pancakes nationwide due to potential Listeria monocytogenes contamination. Affected products have batch codes starting with 2C and Best By dates between October 1, 2024 and October 11, 2025.
Product
BREAKFAST BEST 8/33oz GRDL PNCK BDAY-BKBST UPC 4061459959116
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0157-2025·2024-12-04
Signature Select Griddle Pancakes Recalled for Potential Listeria Contamination
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.
Product
SIGNATURE SELECT 12/14.1oz GRDL PNCK MINI-SIGSL UPC 021130095889
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0203-2025·2024-12-04
GOOD & GATHER griddle waffles recalled for potential Listeria contamination
GOOD & GATHER and 365 ORGANIC brand griddle waffles are being recalled due to potential Listeria monocytogenes contamination. Affected products have batch codes starting with 2C and best-by dates from October 1, 2024 to October 11, 2025.
Product
GOOD & GATHER 12/9oz GRDL WFL MINI BLBRY ORG-GDGTR UPC 085239343012 365 ORGANIC 12/9oz GRDL WFL MINI BLBRY ORG - 365OR UPC 099482437008
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0191-2025·2024-12-04
Griddle Waffles Recalled for Potential Listeria Contamination
Multiple brands of cinnamon griddle waffles are being recalled due to potential Listeria monocytogenes contamination. Approximately 9.9 million cases are affected.
Product
WESTERN FAMILY 12/280g GRDL WFL CIN - WSTCN UPC 062639310134 GREAT VALUE 12/280g GRDL WFL CIN - GRVLC UPC 681131811712 SELECTION 12/280g GRDL WFL CIN - SLCTN UPC 059749950640 COMPLIMENTS 12/280g GRDL WFL CIN - CMPLM UPC 055742500516 KROGER 12/12.3oz GRDL WFL CIN - KROGR UPC 01111
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0067-2025·2024-12-04
Menthol Patch Recall Due to Manufacturing Quality Deviations
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.
Product
HEALTHWISE MENSTRUAL PAIN RELIEF PATCH — HEALTHWISE MENSTRUAL PAIN RELIEF PATCH (MENTHOL)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0064-2025·2024-12-04
Absorbine Jr Pain Relieving Knee Patch recalled for manufacturing deviations
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.
Product
ABSORBINE JR PAIN RELIEVING KNEE PATCH, Camphor 7%, Menthol 7%, packaged in a) 1 patch (UPC 8 89476 41251 3) and b) 6 patches (UPC 8 89476 41306 0), Distributed By: Absorbine Jr., LLC, Chattanooga, TN 37402
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0070-2025·2024-12-04
JR Watkins Menthol Pain Relief Patches Recalled for Manufacturing Deviations
JR Watkins Cooling Pain Relief Patches are being recalled due to manufacturing process deviations identified during production.
Product
JR WATKINS COOLING PAIN RELIEF PATCHES, Menthol 7.5%, 5 patches per box, Distributed By: J.R. Watkins, LLC, Oakland, CA 94612 UPC 8 56294 00878 5
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0554-2025·2024-12-04
Shimadzu Autosampler Devices Subject to Water Damage Affecting Main Board
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.
Product
Autosampler, Models: SIL-40C XR CL, SIL-40C X3 CL
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0073-2025·2024-12-04
FDA Drug Recall: LICEOUT Liquid Lice Treatment for Manufacturing Violations
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.
Product
LICEOUT, Liquid Lice Treatment for Human Use, Contents: 1 FL. OZ. (29.6 mL) per sachet, Distributed By: Bob Barker Company, Inc., 7925 Purfoy Road, Fuquay-Varina, NC 27526. NDC: 53427-124-01
Category
Drug
Distribution
0 states
ModerateFDA (Drugs)·D-0075-2025·2024-12-04
Menthol pain relief patches recalled for manufacturing practice violations
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.
Product
Cooling Menthol Extra Strength Pain Relief Patch, Menthol 7.5%, packaged in box of 5, Distributed by J.R. Watkins LLC, Oakland CA 94612 UPC 8 56294 00878 5, NDC 72342-100-05
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0072-2025·2024-12-04
Parche Leon pain relief patches recalled for manufacturing deviations
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.
Product
PARCHE LEON — PARCHE LEON (CAPSAICIN, CAMPHOR, MENTHOL)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0062-2025·2024-12-04
Topical menthol back patch recalled for manufacturing deviations
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.
Product
ABSORBINE jr. Extra Large BACK PATCH, Menthol 5%, 1 extra large patch per box, Distributed By: Absorbine Jr., LLC, Chattanooga, TN 37402 UPC 8 89476 41218 6, UPC 8 89476 41236 0
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0550-2025·2024-12-04
GE Proteus XR/A radiographic system Wall Stand cable maintenance recall
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.
Product
GE Proteus XR/A radiographic system
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0552-2025·2024-12-04
Heart Device Transmitter Fails to Update Software After Power Interruption
Abbott Medical's Merlin@home transmitter cannot upgrade to current software after power interruptions during prior downloads. This affects remote heart device monitoring systems.
Product
Merlin@home with the MerlinOnDemand capability Transmitter REF EX1150 Merlin@home with the MerlinOnDemand" (MoD) capability is a transmitter configured for multiple patient use. It can receive information from an implantable heart device in unpaired mode. With MoD capability
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0520-2025·2024-12-04
GE SIGNA and DISCOVERY PET/MR Scanners Recalled for Elevated Acoustic Noise
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.
Product
Tomographic Imager Combining Emission Computed Tomography With Nuclear Magnetic Resonance: 1) SIGNA PET/MR, 2) DISCOVERY PET/MR,
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0074-2025·2024-12-04
Drug Lice Treatment Recalled Due to Manufacturing Practice Violations
Neogen Corporation has voluntarily recalled LICEOUT liquid lice treatment due to manufacturing practice violations. The recall affects 8,328 jugs distributed to institutions.
Product
LICEOUT, Liquid Lice Treatment for Human Use, Contents: 128 FL OZ. (3785.4 mL mL) per jug, Distributed By: Bob Barker Company, Inc., 7925 Purfoy Road, Fuquay-Varina, NC 27526. NDC: 53247-124-02
Category
Drug
Distribution
0 states
ModerateFDA (Devices)·Z-0551-2025·2024-12-04
Abbott Merlin@home Cardiac Monitoring Transmitters Fail to Update After Power Loss
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.
Product
Merlin@home Transmitter REF EX1100 The Merlin@home" (M@h) transmitter is intended to transfer stored data from the patient s implanted heart device to Merlin.net" Patient Care Network (PCN) to facilitate remote monitoring by using inductive (EX1100 Model) or RF telemetry (E
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0071-2025·2024-12-04
FDA Recalls Cheeky Bonsai Menthol Pain Relief Patches for Manufacturing Deviations
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.
Product
CHEEKY BONSAI PAIN RELIEF PATCHES, Menthol 10%, 4 patches per box, Distributed by Cheeky Bonsai, San Francisco, CA UPC 8 60006 57564 9
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0558-2025·2024-12-04
Medline Endo Kit Recall: Missing Lot and Expiration Date Labels
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.
Product
ENDO KIT, Medline Kit SKU DYKE1577A, Component Number 57469, 10 per case; Medline Convenience Kits containing Single Use Biopsy Valve MAJ-1555
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0523-2025·2024-12-04
Z-800WF Infusion Pumps Recalled for Software Incompatibility Issue
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.
Product
Brand Name: Z-800 Infusion System Product Name: Z-800WF Model/Catalog Number: Z-800WF. The Z-800 Infusion system is intended to provide intravenous infusion of parenteral fluids, blood, and blood products to a patient under the direction or supervision physician or other certi
Category
Medical Device
Distribution
8 states
ModerateFDA (Drugs)·D-0066-2025·2024-12-04
FDA Recalls Menthol Medicated Patches Due to Manufacturing Deviations
FDA recalls THERA CARE COLD HOT MEDICATED PATCH (menthol 5%) due to manufacturing practice deviations. The voluntary recall affects 279,936 patches distributed nationwide.
Product
THERA CARE COLD HOT MEDICATED PATCH — THERA CARE COLD HOT MEDICATED PATCH (MENTHOL)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0068-2025·2024-12-04
Equate Maximum Strength Lidocaine Pain Relieving Patches Recalled for Manufacturing Deviations
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.
Product
EQUATE PAIN RELIEVING PATCHES — EQUATE PAIN RELIEVING PATCHES (LIDOCAINE 4%)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0065-2025·2024-12-04
THERACARE Lidocaine Pain Relief Patches Recalled for Manufacturing Deviations
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.
Product
THERACARE MAXIMUM STRENGTH PAIN RELIEF PATCH — THERACARE MAXIMUM STRENGTH PAIN RELIEF PATCH (LIDOCAINE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0069-2025·2024-12-04
LILAS Feminine Pain Relief Patch recalled for manufacturing violations
Unexo Life Sciences is voluntarily recalling LILAS Feminine Pain Relief Patch nationwide due to manufacturing practice deviations affecting 363,300 patches.
Product
LILAS Feminine Pain Relief Patch, Menthol 10%, a) 5 patches per box (UPC 7 87099 48212 1) and 10 patches per box (UPC 7 87099 48211 4), Distributed by: Lilas Wellness, Inc., Beaverton, Oregon 97008-7105
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-0557-2025·2024-12-04
Tempus LS-Manual Defibrillator Recalled for Incorrect Servicing Labels
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.
Product
Tempus LS-Manual Defibrillator Model 00-3020 The Tempus LS-Manual is a defibrillator that can deliver a shock in manual or Pacemaker mode
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·24V908000·2024-12-03
2025 Kenworth T880 steering fasteners may fail and cause crashes
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.
Product
PETERBILT — PETERBILT, KENWORTH 520, T480, 548, 367
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V907000·2024-12-03
Nova Bus recalls 2022-2024 LFS buses for wheelchair restraint defect
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.
Product
NOVA BUS — NOVA BUS LFS
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V906000·2024-12-03
International Recalls 2025 EMV Vehicles Due to Missing Defrost Circuit Breaker
International is recalling 2025 EMV vehicles because a missing circuit breaker may cause the windshield defrosting system to fail, reducing visibility.
Product
INTERNATIONAL — INTERNATIONAL EMV
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·24V905000·2024-12-02
Pierce Fire Trucks Recalled for Incompatible Front Tires and Wheels
Pierce is recalling 2023-2024 Velocity, Enforcer, and Quantum fire trucks because front steer axle tires are incompatible with the wheels, increasing crash risk.
Product
PIERCE — PIERCE VELOCITY, ENFORCER, QUANTUM
Category
Vehicle
Distribution
Distributed nationwide
HighUSDA FSIS·PHA-12022024-01·2024-12-02
USDA Issues Public Health Alert for Ineligible Imported Pork Mortadella
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.
Product
FSIS Issues Public Health Alert for Ineligible Pork Products Imported From Ecuador
Category
Food
Distribution
1 state
HighNHTSA·24V903000·2024-12-02
Kenworth and Peterbilt Trucks Recalled for Insufficient Axle Bearing Lubrication
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.
Product
PETERBILT — PETERBILT, KENWORTH 548, T380, T480, 536
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V904000·2024-12-02
Tesla Recalls 2024 Model X Vehicles Due to Flickering Headlights
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.
Product
TESLA — TESLA MODEL X
Category
Vehicle
Distribution
Distributed nationwide

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