State

New Jersey product recalls

73,737 recalls have nationwide distribution and so reach New Jersey. 9,780 additional recalls listed New Jersey specifically in their distribution scope.

What the numbers show

Total: 9,780
Critical: 1,246
Severe: 2,942
Most recent: 2026-10-28

Of the 9,780 recalls naming New Jersey we have scored against our rubric, 1,246 (13%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,942 (30%) are Severe.

Which agencies issued them

These figures cover only the 9,780 recalls whose distribution notice names New Jersey specifically. The 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

30226–30250 of 83517

HighFDA (Devices)·Z-0617-2021·2020-12-23
Biomet Cannulated Screw System Recalled for Potential Sterile Seal Breach
Biomet is recalling specific lots of cannulated screw systems because a breach in the sterile packaging seal could lead to loss of sterility.
Product
4.0/5.0mm Cannulated Screw System, BCS Cannulated Screw System (3.0, 4.0/5.0, 6.5/8.0mm), Item numbers 110009810, 110009821, 110009825, 110009852 - Product Usage: Fracture fixationof small bones, small bone fragements and long bones.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0628-2021·2020-12-23
Biomet Hip Prosthesis Recall for Potential Sterile Seal Breach
Biomet is recalling specific lots of RINGLOC BIPOLAR Hip System components due to a potential breach in the sterile seal, which could lead to loss of sterility.
Product
RINGLOC BIPOLAR Hip System Bi Polar Locking Ring, Item number 11-165304 - Product Usage: Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate, Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented, Prosthesis, Hip…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0588-2021·2020-12-23
BD PrecisionGlide Needles Recalled Due to Blood Contamination
Becton Dickinson is recalling BD PrecisionGlide needles because blood was found on the cannulas, posing a potential infection risk if not noticed by clinicians.
Product
BD PrecisionGlide Needle 30G x 1/2 (0.3 mm X 13mm) REF 305106 - Product Usage: used for general purpose injection and aspiration of fluids from vials, ampoules and parts of the body below the surface of the skin.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·20V810000·2020-12-23
International DuraStar and WorkStar Engine Control Software Defect Recall
Navistar recalls 17,213 2014-2021 International commercial trucks with an engine control defect. The software flaw can cause unexpected vehicle movement when parked with the PTO engaged, risking crashes and injury.
Product
INTERNATIONAL — INTERNATIONAL MV, DURASTAR, WORKSTAR, HV
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0636-2021·2020-12-23
Kowa VK-2s Software Recall for Potential Patient Data Deletion
Kowa Optimed Inc is recalling VK-2s software installed on nonmyd WX Retinal Cameras because a defect may cause the deletion of all patient information, potentially delaying treatment.
Product
Kowa VK-2s software Version 10.0.4.0, Product code 04987646809500 installed on Kowa nonmyd WX Retinal Cameras - Product Usage: is indicated for acquiring, displaying and storing image data from KOWA s mydriatic and non-mydriatic ophthalmic cameras.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·20V811000·2020-12-23
GM Recalls Bolt EV and Other Vehicles for Seat Belt Attachment Defect
General Motors is recalling multiple 2020-2021 vehicles due to incorrect bolts used to secure seat belts. Improperly fastened seat belts may fail to properly restrain occupants in a crash.
Product
CHEVROLET — CHEVROLET, CADILLAC, GMC SUBURBAN, ESCALADE NA, COLORADO, SILVERADO 3500
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0565-2021·2020-12-23
Terumo Capiox FX25 Advance Oxygenator Recall for Configuration Error
Terumo is recalling Capiox FX25 Advance Oxygenators because they may have the incorrect East or West configuration. The recall affects 5,079 units distributed in the US and abroad.
Product
(1) Capiox FX25 (West) Advance Oxygenator- with left port, 4-liter Reservoir, XC modified to Advance, Sterile Catalog Number: 3CX*FX25RWC (2) Capiox FX25 (East) Advance Oxygenator - FX25 with right port, 4-liter Reservoir, XC modified to Advance Catalog Number…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0152-2021·2020-12-23
Taro Recalls HEB Clotrimazole Cream Due to Impurity
Taro Pharmaceuticals is recalling HEB Clotrimazole Cream 1% because an unknown degradation impurity was detected slightly above the specification limit.
Product
HEB — HEB (CLOTRIMAZOLE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0634-2021·2020-12-23
Roche Recalls Tina-quant C-Reactive Protein Gen.3 Reagents Due to Cross-Contamination
Roche is recalling Tina-quant C-Reactive Protein Gen.3 reagents due to cross-contamination causing invalid calibrations and low quality control recovery.
Product
Tina-quant C-Reactive Protein Gen.3, Catalog number 05172373190 - Product Usage: the in vitro quantitative determination of CRP in human serum and plasma on Roche automated clinical chemistry analyzers.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0157-2021·2020-12-23
Taro Recalls Clotrimazole Cream Due to Unknown Degradation Impurity
Taro Pharmaceuticals is recalling Best Choice Clotrimazole Cream USP 1% because an unknown degradation impurity was detected slightly above the specification limit.
Product
Best Choice, Clotrimazole Cream, USP 1%, Antifungal, NET WT 0.5 OZ (14.2g), Distributed by: Valu Merchandisers, CO . 5000 Kansas Ave. Kansas City, KS 66106 Made in Canada. UPC 0-70038-20355-1
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0167-2021·2020-12-23
AvKARE Recalls Sildenafil Tablets Due to Packaging Mix-Up with Trazodone
AvKARE Inc. is recalling 38,715 bottles of Sildenafil 100 mg tablets because they were inadvertently packaged with trazodone at a third-party facility.
Product
Sildenafil Tablets USP 100 mg, Rx Only, 100-count Bottle, Manufactured for: AvKARE Pulaski, TN 38478, NDC 42291-748-01.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0156-2021·2020-12-23
Taro Recalls Rite Aid Clotrimazole Cream Due to Impurity
Taro Pharmaceuticals is recalling Rite Aid Clotrimazole Cream because an unknown degradation impurity was detected slightly above the specification limit.
Product
RiteAid Pharmacy RIngworm Cream, Clotrimazole Cream USP, 1%, Antifungal NET W 0.5 oz. (14.2g), Distributed by: Rite Aid, 30 Hunter Lane, Camp Hill, PA 17011 Made in Canada. UPC 0 11822 53812 1
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0155-2021·2020-12-23
Taro Recalls Kroger Clotrimazole Cream Due to Impurity
Taro Pharmaceuticals is recalling Kroger Clotrimazole Cream 1% because an unknown degradation impurity was detected slightly above the specification limit.
Product
KROGER — KROGER (CLOTRIMAZOLE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0635-2021·2020-12-23
Helena Laboratories Recalls K-ACT Actalyke Clotting Test Tubes
Helena Laboratories is recalling K-ACT Actalyke Clotting Test Tubes due to complaints of cracked or split caps.
Product
K-ACT Actalyke Clotting Test Tubes that are used in the: ACTALYKE XL ACTIVATED CLOTTING TIME ANALYZER, and ACTALYKE MINI ACTIVATED CLOTTING TIME TEST SYSTEM.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0169-2021·2020-12-23
Hikma Recalls Sodium Chloride Injection Vials Due to pH Failures
Hikma Pharmaceuticals is recalling 1.3 million vials of Sodium Chloride Injection USP 0.9% because pH test results were out of specification.
Product
SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0615-2021·2020-12-23
Medline Recalls RevMedX Trauma Dressings Due to Package Seal Integrity Issues
Medline Industries is recalling RevMedX Trauma Dressings because of package seal integrity issues. The recall affects 15,780 units distributed in the US and several international countries.
Product
RevMedX Trauma Dressings are packaged in a Tyvek Peel pouch, 1 Trauma Dressing per Tyvec Peel Pouch, 30 Pouches per Case; Sterile - Product Usage: are intended to absorb exudates.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0612-2021·2020-12-23
Medtronic Percept PC Neurostimulator Recall Due to Software Connection Failure
Medtronic is recalling 12 Percept PC Implantable Neurostimulators because a software anomaly in the A620 Patient Programmer prevents connection to the device.
Product
Percept PC Implantable Neurostimulator (INS) - Product Usage: The Percept PC is a neurostimulation device for deep brain stimulation therapy. It is indicated for DBS treatment for Parkinson s disease, essential tremor, dystonia, obsessive-compulsive disorder, and epilepsy.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0180-2021·2020-12-23
Fusion Health Recalls Pharmorigins Core Supplement for Unapproved Additive
Fusion Health and Vitality LLC is recalling Pharmorigins Core dietary supplements due to the unapproved use of a food additive and unapproved marketing statements.
Product
PHARMORIGINS CORE with Natural Orange Flavor NATURAL ENERGY and IMMUNE HEALTH Dietary Supplement 30 Servings (45g) Supplement Facts***Hordenine HCL*** Manufactured by: Fusion Health Vitality, LLC 1360 Union Hill Road, Suite 11B Alpharetta, GA 30004 888.964.5327 UPC 7 28028 21054…
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0159-2021·2020-12-23
Taro Recalls Clotrimazole Cream Due to Unknown Degradation Impurity
Taro Pharmaceuticals is recalling specific lots of Clotrimazole Cream USP 1% because an unknown degradation impurity was detected slightly above the specification limit.
Product
Athlete's Foot Cream, Clotrimazole Cream USP, 1%, Antifungal Cream, NET WT 1 oz (30 g), Distributed by: Taro Pharmaceuticals U.S.A. Inc. Hawthorne, NY 10531. Made in Canada. UPC 3 51672 20022 0
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0570-2021·2020-12-23
Zimmer Biomet Recalls Polaris Spinal System Screws for Labeling Update
Zimmer Biomet is updating instructions for Polaris and Cypher spinal screws to warn against using them with direct current stimulation due to construct failure risks.
Product
Polaris 5.5 Spinal System and Polaris 5.5/Cypher Spinal System, Thoracolumbosacral pedicle screw system
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0158-2021·2020-12-23
Taro Recalls TopCare Clotrimazole Cream Due to Impurity
Taro Pharmaceuticals is recalling TopCare Clotrimazole Cream because an unknown degradation impurity was detected slightly above the specification limit.
Product
TOPCARE — TOPCARE (CLOTRIMAZOLE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0568-2021·2020-12-23
Galt Medical Recalls Centeze Centesis Catheters Due to Tip Geometry Defect
Galt Medical Corporation is recalling 9,920 Centeze Centesis Catheters because a manufacturing issue resulted in incorrect tip geometry, specifically a thicker wall and more obtuse tip angle.
Product
Centeze Centesis Catheter, 6F, 10cm, 18Ga, 12cm, REF DRC-002-06 Centeze Centesis Catheter, 6F, 10cm, 18Ga, 12cm, REF DRC-006-16
Category
Medical Device
Distribution
9 states
ModerateFDA (Drugs)·D-0154-2021·2020-12-23
Taro Recalls Kroger Clotrimazole Cream Due to Impurity
Taro Pharmaceuticals is recalling Kroger Athlete's Foot Cream because an unknown degradation impurity was detected slightly above the specification limit.
Product
KROGER — KROGER (CLOTRIMAZOLE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0146-2021·2020-12-23
Zydus Recalls Lansoprazole Tablets for Failed Dissolution Specifications
Zydus Pharmaceuticals is recalling 22,848 cartons of Lansoprazole 30 mg tablets nationwide because they failed to meet dissolution specifications.
Product
LANSOPRAZOLE — LANSOPRAZOLE (LANSOPRAZOLE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0151-2021·2020-12-23
Taro Recalls Clotrimazole Cream Due to Unknown Impurity
Taro Pharmaceuticals is recalling Equate Athlete's Foot cream because an unknown impurity was detected above specification limits.
Product
CLOTRIMAZOLE — CLOTRIMAZOLE (CLOTRIMAZOLE)
Category
Drug
Distribution
Distributed nationwide