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.

4,754 stored notices name New Jersey, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,132 notices were distributed nationwide, so they reach New Jersey too — those are in the archive.

Medical devices

Reported Jul 8, 2015

Infinite F500, in vitro diagnostic. Product Usage: The Tecan Infinite F500 is a multifunctional microplate reader with…

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

Tecan US, Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 8, 2015

Natural Knee II Revision Femoral Stem, 125mm, item 6215-12-185. packaged in configuration 803/791. Knee Prosthesis…

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

Zimmer, Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 1, 2015

Raw Macadamia Nuts, packaged in 8 oz. plastic cup, packaged under the Aurora and private labels as follows:Belmont…

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

Aurora Products, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jul 1, 2015

LapSac Surgical Tissue Pouch. The current intended use for the LapSac Surgical Tissue Pouch is for isolating tissue…

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

Cook Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 1, 2015

Cambridge House Royal Smoked Salmon Sliced Side Products are packaged in Reduced Oxygen Package (ROP). Product is…

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

The Santa Barbara Smokehouse, Inc.

8 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 1, 2015

Fortex" Pedicle Screw System Continuous Radius Rod 5.5 - 50mm, X-Spine Systems, Inc., 452 Alexandersville Road…

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

X Spine Systems Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 24, 2015

Amerigel Hydrogel Gauze Dressing 2 x 2, A5002. Wound Management.

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

Amerx Health Care Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 24, 2015

BVI Custom Eyes¿ Ophthalmic Procedure Kits with the component -Devon Light Glove Part Number: 584569 Ophthalmic…

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

Beaver-Visitec International Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 24, 2015

Vanguard M Unicondylar Tibial Trial For use during knee joint replacement.

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

Biomet, Inc.

FDA (openFDA device enforcement)

Food

Reported Jun 24, 2015

Byrds Famous Cookies, Benne Bits, Net Wt. 6 oz. tins, UPC: 0-74882904651-8, Byrd Cookie Company, P.O. Box 1308,…

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

Byrd Cookie Co.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jun 24, 2015

MILEX OMNIFLEX DIAPHRAGM SIZE 80 Model: MXWF80

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

CooperSurgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 24, 2015

HeartWare Ventricular Assist System (HVAD). Catalog #'s US: 1101 and 1103 / OUS: 1100,1101,1102,1104,1104JP and 1205.…

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

HeartWare Inc.

FDA (openFDA device enforcement)

Drugs

Reported Jun 24, 2015

Foradil Aerolizer (formoterol fumarate inhalation powder) 12 mcg per capsule, 12 Capsules (Blister strips of 6) per…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Novartis Pharmaceuticals Corp.

1 more product in this recall

FDA (openFDA drug enforcement)

Medical devices

Reported Jun 24, 2015

Navigation System II-Cart, 7700-100-000 with Articulated Arm Camera, 7700-103-001 and Articulated Arm Camera,…

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

Stryker Instruments Div.

FDA (openFDA device enforcement)

Food

Reported Jun 24, 2015

Hacizade Pismaniye Pashmak (Cotton Candy with Rose), Net Wt. 250-g (8.80-oz.), UPC 8697407913372

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Turkana Food Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jun 17, 2015

Extentrac Elite product brochure DCN: 13-001, 09-001 (Powered decompression table, for traction)

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

Advanced Back Technologies, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 17, 2015

AGFA DX-D 100 is a mobile digital radiography x-ray system

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

AGFA Healthcare Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 17, 2015

BBL Port A Cul tubes, catalog number 221606. Patient sample collection tubes. BBL Port A Cul tubes, jars and vials…

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

Becton Dickinson & Co.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 17, 2015

Roscoe Mini Neb Compressor User Manual for the NEB-ROS Product Usage: Inhaler therapy that converts liquid medicine…

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

Compass Health Brands

FDA (openFDA device enforcement)

Medical devices

Reported Jun 17, 2015

GE OEC Brivo 865 plus, Mobile X-ray system laser aimer assemblies (part number 520002DW)

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

GE OEC Medical Systems, Inc.

FDA (openFDA device enforcement)

Food

Reported Jun 17, 2015

Golden Krust SOYA PATTIES, NET WT. 17.2 LBS, 50 UNBAKED, KEEP FROZEN

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

Golden Krust Caribbean Bakery, Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Food

Reported Jun 17, 2015

1-lb, 2-lb and 10-lb bags of Soybean Sprouts in clear plastic bags labeled GOODSEED Soy Bean Sprouts Keep Refrigerated

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

Good Seed, Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jun 17, 2015

HeartWare Ventricular Assist System (HVAD). Catalog #'s US: 1101 and 1103 / OUS: 1100, 1101,1102,1104,1104JP and 1205.…

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

HeartWare Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 17, 2015

FLOW-i Anesthesia System The FLOW-i Anesthesia System is intended for use administering inhalation anesthesia on…

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

Maquet Cardiovascular US Sales, LLC

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.