State

New Jersey product recalls

73,576 recalls have nationwide distribution and so reach New Jersey. 9,773 additional recalls listed New Jersey specifically in their distribution scope.

What the numbers show

Total: 9,773
Critical: 1,249
Severe: 2,939
Most recent: 2026-10-14

Of the 9,773 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 2,939 (30%) are Severe.

Which agencies issued them

These figures cover only the 9,773 recalls whose distribution notice names New Jersey specifically. The 73,576 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

151–175 of 83349

HighFDA (Food)·H-0026-2027·2026-10-14
J K Patisserie Chocolate Chip Cookies Recalled for Undeclared Soy
J K Patisserie & Bakery LLC is recalling 610 units of chocolate chip cookies sold in New York and New Jersey because soy was not declared in the Contains statement.
Product
Chocolate Chip Cookies packaged in a cardboard box; Ingredients: King Midas Special (Wheat flour, niacin, reduced iron, thiamine mononitrate, riboflavin, folic acid, malted barley flour), Dark Chocolate Chip (sugar, unsweetened chocolate, cocoa butter, soy lecithin, ground…
Category
Food
Distribution
2 states
HighFDA (Devices)·Z-0073-2027·2026-10-14
Steris VERIFY Dual Species Biological Indicator Recall for Spore Population Issues
Steris Corporation is recalling VERIFY Dual Species Self-Contained Biological Indicators because the spore population may fall below specifications, potentially leading to false sterilization results.
Product
VERIFY Dual Species Self-Contained Biological Indicator Model/Catalog Number: S3061
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·N/A·2026-10-14
Beak & Skiff Alcohol Antiseptic Sanitizer recalled for acetaldehyde contamination
Beak & Skiff Sanitizer Alcohol Antiseptic 80% is being recalled because FDA analysis found acetaldehyde above specification limits in the product. The recall affects bottles distributed in New York and through online sales.
Product
Tri-Immune Boost (Glutathione: 200 mg, Ascorbic Acid: 200 mg, Zinc: 2.5 mg), 30 mL vial, Rx only, Centric Compounding, 7447 Harwin Dr. Suite 111, Houston, TX 77036
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0101-2027·2026-10-14
Avid Medical Recalls 30 DAVINCI LAP/GYN Kits for Lubricant Contamination
Avid Medical, Inc. is recalling 30 DAVINCI LAP/GYN kits (Model WRNM037-16) because they may be contaminated with a lubricant used during manufacturing.
Product
DAVINCI LAP/GYN; Model/Item Number (Kit): WRNM037-16;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0090-2027·2026-10-14
Onkos My3D Personalized Pelvic Implant Recalled for Distribution Error
Onkos Surgical is recalling My3D Personalized Pelvic Implants that were inadvertently mixed up and distributed to incorrect customers.
Product
Onkos Surgical Inc. My3D Personalized Pelvic Implant, Porous, Left REF PV-ACREC-04M
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0095-2027·2026-10-14
AVID Medical Recalls 33 Endovascular Packs Due to Lubricant Contamination
AVID Medical, Inc. is recalling 33 Endovascular Packs (Model VAPX014-04) because they may be contaminated with a lubricant used during manufacturing.
Product
ENDOVASCULAR PACK; Model/Item Number (Kit): VAPX014-04;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0103-2027·2026-10-14
AVID Medical Recalls Urology Kits for Potential Lubricant Contamination
AVID Medical, Inc. is recalling 20 Urology Major kits (Model WRNM058-10) because they may be contaminated with a lubricant used during manufacturing.
Product
UROLOGY MAJOR; Model/Item Number (Kit): WRNM058-10;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0082-2027·2026-10-14
DRG Sperm Ab ELISA Recalled for Potential False Negative Results
DRG International is recalling Sperm Ab ELISA kits due to a potential for false negative patient results. The recall covers 211 units distributed in the US and several international countries.
Product
Sperm Ab ELISA; Model/Catalog Number: EIA-1826; Product Description: Sperm Ab ELISA (96 well plate test);
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0013-2027·2026-10-14
Preferred Pharmaceuticals Recalls Lidocaine Ointment Due to Content Uniformity Failures
Preferred Pharmaceuticals is recalling Lidocaine Ointment USP, 5% due to failed content uniformity specifications. The product is distributed nationwide.
Product
Lidocaine Ointment USP, 5% (Generic for Xylocaine), packaged in a 50 g jar, Rx only, Mfg: Taro Pharmaceuticals U.S.A., Inc., Prod# (NDC): 68788-7865-05
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0102-2027·2026-10-14
AVID Medical Recalls Heart Prep Trays for Lubricant Contamination
AVID Medical, Inc. is recalling 96 Heart Prep Trays (Model MECV97W) because they may be contaminated with a lubricant used during manufacturing.
Product
HEART PREP TRAY; Model/Item Number (Kit): MECV97W;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0091-2027·2026-10-14
Onkos Surgical Recalls My3D Personalized Pelvic Implant Due to Distribution Error
Onkos Surgical is recalling My3D Personalized Pelvic Implants that were inadvertently mixed up and distributed to incorrect customers.
Product
Onkos Surgical Inc. My3D Personalized Pelvic Implant, Porous, Left REF PV-ACREC-04M
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0014-2027·2026-10-14
Cipla Recalls Fosfomycin Tromethamine Due to Impurity Specification Failures
Cipla USA, Inc. is recalling specific lots of Fosfomycin Tromethamine granules because they failed impurity and degradation specifications.
Product
FOSFOMYCIN TROMETHAMINE — FOSFOMYCIN TROMETHAMINE (FOSFOMYCIN TROMETHAMINE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0077-2027·2026-10-14
Halyard Laparoscopy Comprehensive Pack II Recalled for Latex Content
GRI Medical is recalling Halyard Laparoscopy Comprehensive Pack II kits because they contain a latex urethral catheter despite being labeled as latex-free.
Product
HALYARD Laparoscopy Comprehensive Pack II REF: 49332
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0100-2027·2026-10-14
AVID Medical Recalls Plastic Trays Due to Lubricant Contamination
AVID Medical, Inc. is recalling 28 units of EURO053 plastic trays potentially contaminated with manufacturing lubricant. The units were distributed in AZ, CA, FL, MD, NE, and TX.
Product
PLASTICS TRAY; Model/Item Number (Kit): EURO053;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0083-2027·2026-10-14
Beckman Coulter Recalls DxC 500i Clinical Analyzer Modules Due to Software Error
Beckman Coulter is recalling DxC 500i Clinical Analyzer Modules because a software issue can cause test units to revert to defaults without warning, potentially resulting in falsely elevated reported results.
Product
DxC 500i Clinical Analyzer Modules: 1. DxC 500 AU Module w/ISE, DxC 500i, Part No. C63522 2. DxC 500 AU Module, DxC 500i, Part No. C63521 3. Access 2 Module, DxC 500i, Part No. C13252
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0097-2027·2026-10-14
Avid Medical Recalls Open Heart Kits Due to Lubricant Contamination
Avid Medical is recalling 124 Open Heart CFH kits because they may be contaminated with a lubricant used during manufacturing.
Product
PACK OPEN HEART CFH; Model/Item Number (Kit): 1. UFCF004-06, 2. UFCF004-07;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0092-2027·2026-10-14
Avid Medical Recalls Davinci Trucustom Bundles Due to Lubricant Contamination
Avid Medical, Inc. is recalling 144 Davinci Trucustom Bundles because they may be contaminated with a lubricant used during manufacturing.
Product
DAVINCI TRUCUSTOM BUNDLE; Model/Item Number (Kit): 1. SAMM064-27, 2. SAMM064-28;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0080-2027·2026-10-14
Limitless Cryo Spa LLC Recalls Glypto Devices for Lack of 510(k) Clearance
Limitless Cryo Spa LLC is recalling 219 Glypto Devices and Cryo Machines because they lack FDA 510(k) clearance. The recall covers units distributed nationwide.
Product
Glypto Device, Glypto Cryo Machine;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0096-2027·2026-10-14
AVID Medical Recalls Craniotomy Packs Due to Potential Lubricant Contamination
AVID Medical, Inc. is recalling 10 Craniotomy Packs (Model WRNM035-20) because they may be contaminated with a lubricant used during manufacturing.
Product
CRANIOTOMY PACK; Model/Item Number (Kit): WRNM035-20;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0093-2027·2026-10-14
AVID Medical Recalls GYN Laparoscopy Kits for Potential Lubricant Contamination
AVID Medical, Inc. is recalling 134 GYN Laparoscopy/Laparotomy kits due to potential contamination with a manufacturing lubricant.
Product
GYN LAPAROSCOPY/LAPAROTOMY; Model/Item Number (Kit): 1. WRNM002-15, 2. FBCH108-03;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0099-2027·2026-10-14
AVID Medical Recalls 15 Laparoscopic Prostatectomy Kits for Lubricant Contamination
AVID Medical, Inc. is recalling 15 laparoscopic prostatectomy kits because they may be contaminated with a lubricant used during manufacturing.
Product
LAPAROSCOPIC PROSTATECTOMY; Model/Item Number (Kit): NIHB0036-07;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0076-2027·2026-10-14
Quantum Ops Recalls ADAPTABLE Beach Chair Surgical Patient Positioners
Quantum Ops Inc is recalling 266 ADAPTABLE Beach Chair surgical patient positioners due to a manufacturing issue involving inadequate welds in the patient head positioning system.
Product
Brand Name: ADAPTABLE Beach Chair Product Name: Beach Chair surgical patient positioner Model/Catalog Number: 804-33-300 (Enovis); 3105-400-030 (Stryker); internal BC-0001 / BC-0220 Software Version: N/A Product Description: Surgical beach-chair positioner that mounts to…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0094-2027·2026-10-14
Avid Medical Recalls Adult Heart Tray Shands Jacks Due to Lubricant Contamination
Avid Medical, Inc. is recalling 59 units of Adult Heart Tray Shands Jacks (Model SHND419-08) because they may be contaminated with a lubricant used during manufacturing.
Product
ADULT HEART TRAY SHANDS JACKS; Model/Item Number (Kit): SHND419-08;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0084-2027·2026-10-14
Beckman Coulter DxC 500 AU Clinical Chemistry Analyzers Recalled for Software Error
Beckman Coulter is recalling DxC 500 AU Clinical Chemistry Analyzers due to a software issue that may cause test units to revert to defaults without warning, potentially resulting in falsely elevated reported results.
Product
DxC 500 AU Clinical Chemistry Analyzers: 1. AU w/out ISE, Part No. C63519 2. AU w/ISE, Part No. C63520
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0098-2027·2026-10-14
Avid Medical Recalls Robotic Prostatectomy Packs for Lubricant Contamination
Avid Medical, Inc. is recalling six Robotic Prostatectomy Packs (NAMC423-11) because they may be contaminated with a manufacturing lubricant.
Product
ROBOTIC PROSTATECTOMY PACK; Model/Item Number (Kit): NAMC423-11;
Category
Medical Device
Distribution
Distributed nationwide