State

New Jersey product recalls

73,096 recalls have nationwide distribution and so reach New Jersey. 9,767 additional recalls listed New Jersey specifically in their distribution scope.

What the numbers show

Total: 9,767
Critical: 1,249
Severe: 2,486
Most recent: 2026-09-25

Of the 9,767 recalls naming New Jersey we have scored against our rubric, 1,249 (13%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,486 (25%) are Severe.

Which agencies issued them

These figures cover only the 9,767 recalls whose distribution notice names New Jersey specifically. The 73,096 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

9426–9450 of 82863

HighFDA (Food)·F-0208-2025·2024-12-04
SELECTION and COMPLIMENTS Griddle Waffles Recalled for Listeria Risk
Treehouse Foods is recalling SELECTION and COMPLIMENTS brand griddle waffles nationwide due to potential Listeria monocytogenes contamination. Consumers should not consume the affected products.
Product
SELECTION 1/1.68kg GRDL WFL ORIG-SLCTN UPC 059749904759 COMPLIMENTS 1/1.68kg GRDL WFL ORIG-CMPLM UPC 055742500530 SELECTION 12/280g GRDL WFL ORIG-SLCTN UPC 059749904704 COMPLIMENTS 12/280g GRDL WFL ORIG - CMPLM UPC 055742500547 SELECTION 12/560g GRDL WFL HSTYLE-SLCTN UPC 05974997
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0177-2025·2024-12-04
Griddle waffles recalled for potential Listeria contamination
Treehouse Foods recalls KRUSTEAZ and GOOD & GATHER griddle waffles 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
KRUSTEAZ 1/3.44lb GRDL WFL BLGN DBL CHOC-KRSTZ UPC 00041820818734 KRUSTEAZ 12/13.75oz GRDL WFL BLGN DBL CHOC-KRSTZ UPC 041820818697 GOOD & GATHER 12/13.75oz GRDL WFL BLGN DBL CHOC-GDGTR UPC 085239157930
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0179-2025·2024-12-04
Frozen Griddle and Belgian Waffle Products Recalled for Listeria Contamination Risk
Treehouse Foods is recalling multiple frozen griddle and Belgian waffle brands nationwide due to potential Listeria monocytogenes contamination. No illnesses have been reported.
Product
DUNCAN HINES 1/3.12kg GRDL WFL BLGN ORIG 4IN - DUNHN UPC 091479060275 KRUSTEAZ 1/3.44lb GRDL WFL BLGN ORIG - KRSTZ UPC 686151903331 KRUSTEAZ 1/3.44lb GRDL WFL BLGN ORIG-KRSMX UPC 00686151805307 KRUSTEAZ 1/3.44lb GRDL WFL BLGN ORIG - KRSTZ UPC 686151904017 GORDON CHOICE 1/3.12kg G
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
HighFDA (Food)·F-0199-2025·2024-12-04
Multiple Brands of Griddle Waffles Recalled for Potential Listeria Contamination
Treehouse Foods is recalling griddle waffles sold under multiple store brands due to potential Listeria monocytogenes contamination. The recall affects products distributed nationwide in the USA and Canada.
Product
PICS BY PRICE CHOPPER 6/29.6oz GRDL WFL HSTYLE RF - PRCHP UPC 041735064912 ALWAYS SAVE 12/9.9oz GRDL WFL HSTYLE RF - ASAVE UPC 070038608752 ESSENTIALS 12/9.9oz GRDL WFL HSTYLE RF - ESSEN UPC 607880101874 KROGER 1/4.63lb GRDL WFL HSTYLE RF - KROGR UPC 011110880109 FOOD LION 8/12.3
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0180-2025·2024-12-04
Krusteaz Griddle Waffles Recalled for Potential Listeria Monocytogenes
Treehouse Foods is recalling Krusteaz brand griddle waffles due to potential Listeria monocytogenes contamination. Products were distributed nationwide in the USA and Canada.
Product
KRUSTEAZ 1/3.44lb GRDL WFL BLGN PMPKNN - KRSTZ UPC 686151805277 KRUSTEAZ 12/13.75oz GRDL WFL BLGN PMPKN-KRSTZ UPC 686151805345
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-0196-2025·2024-12-04
Simple Truth Griddle Waffles Recalled for Potential Listeria Contamination
Treehouse Foods is recalling Simple Truth griddle waffles with batch codes starting with 2C due to potential Listeria monocytogenes contamination. Approximately 9.9 million cases were distributed nationwide in the USA and Canada.
Product
SIMPLE TRUTH 12/11.3oz GRDL WFL HSTYLE GF-SMPTR UPC 011110105493
Category
Food
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-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-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-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-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
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-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 (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-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 (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-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-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 (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-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 (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 (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