All recall categories

Recalls distributed in New Jersey

These notices name New Jersey in the distribution list the company gave its agency. That list says where the product was shipped, not where it ended up — a recalled item can travel with a shopper, and some notices list no states at all.

4,816 stored notices name New Jersey, reported between Jun 20, 2012 and Nov 11, 2026. A further 48,765 notices were distributed nationwide, so they reach New Jersey too — those are in the archive.

Food

Reported Feb 5, 2025

WESTCO 3065 GOLDEN BAVARIAN CREME FILLING ARTIFICIALLY FLAVORED Ingredients: Water, Sugar, Modified Food Starch,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

BakeMark USA LLC.

FDA (openFDA food enforcement)

Medical devices

Reported Feb 5, 2025

BD Pyxis MedStation ES AUX Tower REF 343 BD Pyxis " MedStation 4000 AUX Tower REF 314 The BD Pyxis" MedStation ES and…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Food

Reported Feb 5, 2025

Alpha Test 120 count Black labeled plastic bottle, 12 bottles per case of 120 count capsules each per bottle, Store in…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Iovate Health Sciences USA Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Feb 5, 2025

Brand Name: SenTiva" Product Name: VNS Therapy" SenTiva", Model 1000 Model/Catalog Number: 1000 Software Version: NA…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

LivaNova USA, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 5, 2025

Medtronic PIN, 100mm STERILE PERCUTANEOUS REF: 9733235 Medtronic PIN, 150MM, STERILE PERCUTANEOUS REF: 97733236 The…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medtronic Navigation, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 5, 2025

NexGen LCCK Legacy Articular Surface with Locking Screw - Striped Purple/C,D - Height 14 mm, Item Number 00-5994-022-14

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Zimmer, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 29, 2025

BD PCR Cartridges used with MAX System. Model Number: 437519

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Becton Dickinson & Co.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 29, 2025

CODMAN CERTAS Plus Programmable Valve Inline Small Valve Only. Model Number: 828810 Implantable device that provides…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Integra LifeSciences Corp.

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jan 29, 2025

Buttered Vegetables KEEP FROZEN NET WT 10.5 OZ (300g) INGREDIENTS: CARROTS, PEAS, CALIFLOWER, CORN, BUTTER, SUGAR,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Lidl US TRADING

FDA (openFDA food enforcement)

Food

Reported Jan 29, 2025

Mr. Bing brand Sriracha Chili Sauce; 9 oz and 18 oz, in clear PET bottle with green cap; UPC 850044819072 and UPC…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Mr Bing Foods Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jan 29, 2025

VDR4 Phasitron Breathing Circuit Models that contain the venturi component: -A50094 D 5PK, Phasitron Kit, VDR, Single…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Percussionaire Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Jan 29, 2025

Merlin.net Patient Care Network (PCN) Heart Failure Web Application (Model MN6000) (Which interfaces with CardioMEMS"…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

St. Jude Medical

2 more products in this recall

FDA (openFDA device enforcement)

Meat & poultry

Reported Jan 27, 2025

FSIS Issues Public Health Alert for Wegmans Frozen Fully Cooked Chicken Nuggets Due to Possible Extraneous Material…

Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.

Perdue Foods LLC

USDA FSIS

Medical devices

Reported Jan 22, 2025

McKesson Cardiology Hemo software

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

A L I Technologies Ltd.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 22, 2025

Brand Name: Alcon Product Name: Monarch¿ III D Delivery Cartridge Model/Catalog Number: 8065977763 Product Description:…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Alcon Research LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 22, 2025

Idylla INSTRUMENT, IVD, REF P0010. Intended for the detection of nucleic acid targets in various types of human…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Biocartis Nv

FDA (openFDA device enforcement)

Medical devices

Reported Jan 22, 2025

DRG:HYBRiD-XL Insulin. Model/Catalog Number: HYE-5361

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

DRG International, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 22, 2025

Panther Fusion GBS Assay REF PRD-04484 Kit containing Panther Fusion GBS Reagent Cartridge IVD.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Hologic, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 22, 2025

8MM, MONOPOLAR CURVED SCISSORS, IS4000 REF 470179

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Intuitive Surgical, Inc.

38 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 22, 2025

Karl Storz - Endoskope - REF 723400 - Optical Biopsy and Grasping Forceps, CE

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Karl Storz Endoscopy

FDA (openFDA device enforcement)

Medical devices

Reported Jan 22, 2025

Neo-Tee T-Piece Resuscitator, for pediatric emergency respiratory support, Part: 1050805, 1050808, 1050809, 1050810,…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Mercury Enterprises, Inc. dba Mercury Medical

FDA (openFDA device enforcement)

Medical devices

Reported Jan 22, 2025

Implant Epikut S Plus CM 16-Degrees 4,5 X 18,0 mm, REF: ILM 4518N

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Sin Sistema de Implante Nacional S.a

FDA (openFDA device enforcement)

Food

Reported Jan 22, 2025

Yu Yee, Five Spice Powder,1.76oz

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Summit Import Corporation

FDA (openFDA food enforcement)

Medical devices

Reported Jan 15, 2025

AMT Mini Enteral Extension Set, 12" Right Angle Feeding Set with Y-Port. Model/Catalog Number: E6-1222

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Applied Medical Technology Inc.

FDA (openFDA device enforcement)

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Other states

RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.