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 Mar 19, 2014

HER2 Image Analysis Manual Read of HER2 Digital Slides ER/PR Image Analysis IHC PR Breast Tissue Manual Read of Digital…

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

Leica Biosystems Imaging, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 19, 2014

Hand Control 12FR Suction Coagulator with 10 ft cord and holster, Sterile, Disposable, Model Number 0043-25, packaged…

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

Megadyne Medical Products, Inc.

FDA (openFDA device enforcement)

Food

Reported Mar 19, 2014

Nicomex Camaron Entero Whole Shrimp Net Wt 1 oz (28.35 grams). Productos Mexicanos Distributed by Nicomex Inc. 88 First…

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

Nicomex Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Mar 19, 2014

Smith & Nephew RENASYS Soft Port REF: 66800799 (The RENASYS Soft Port Dressing Kits are used in conjunction with…

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

Smith & Nephew Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 19, 2014

4040-2: Umbilical 3 mL Line Draw, Luer lock syringe (heparin concentration: 23.5 I.U. per mL) with Filter-Pro¿ device,…

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

Smiths Medical ASD, Inc.

12 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Mar 12, 2014

Deb-El Foods Dried Whole Eggs Deb El Food Products LLC 2 Papetti Plaza, Elizabeth, NJ 07206

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

Deb-El Food Products, LLC.

FDA (openFDA food enforcement)

Medical devices

Reported Mar 12, 2014

DeRoyal ST. Circumcision Clamp, REF 32-1622, Size 1.3 cm, 1 Per Pack, Rx Only STERILE EO, distributed by DeRoyal…

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

DeRoyal Industries Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 12, 2014

All Elekta digital accelerators with electrons and beam modulator, MLCi/MLCi2, Agility or Asymmetric Heads Product…

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

Elekta, Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 12, 2014

Greatbatch Medical, Offset Cup Impactor. Part Numbers: P9485, T10243, T10281, T10287, T10484, T10491, T10507, T10600,…

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

Greatbatch Medical

FDA (openFDA device enforcement)

Medical devices

Reported Mar 12, 2014

*** 1) List number 126970465 labeled in part: 12697-65 LifeShield LATEX-FREE HEMA; Y-TYPE BLOOD SET, Nonvented, 88 Inch…

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

Hospira Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 12, 2014

Heparin I.V. Flush Syringe is available is pre-filled polypropylene syringes, 100 units/mL, 3 mL fill in a 12 mL…

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

Medefil Incorporated

FDA (openFDA device enforcement)

Food

Reported Mar 12, 2014

Rise n Roll Bakery & Deli, White Powdered Donuts, sold individually and found in 6 count (436 g) UPC Code 6 26570 61744…

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

Rise'n Roll Bakery, LLC

9 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Mar 12, 2014

Triton FP Infusion Pump, Part Number 400000, packaged in boxes. The Triton Volumetric Infusion Pump is indicated for…

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

WalkMed Infusion, LLC

FDA (openFDA device enforcement)

Food

Reported Mar 5, 2014

Kinnikinnick Pancake & Waffle Mix -Weight: 454g/16 oz Cardboard Box UPC 62013310512 2

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

Bozzutos' Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Mar 5, 2014

CSI, Diamondback 360 Coronary Orbital Atherectomy System, Part Number 70058-02, Model Number DBEC-125 Product Usage:…

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

Cardiovascular Systems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 5, 2014

GE Healthcare - Giraffe Warmer;Panda Warmer;Panda iRes Warmer, Giraffe Stand-alone Infant Resuscitation System. Product…

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

GE Healthcare, LLC

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 5, 2014

VITROS Chemistry Products Na+ Slides, manufactured by Ortho Clinical Diagnostics 513 Technology Blvd Rochester, NY…

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

Ortho-Clinical Diagnostics

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 5, 2014

Single and Dual use Emission Computer Tomography gamma cameras (BrightView XCT, BrightView X & BrightView SPECT)…

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

Philips Medical Systems (Cleveland) Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 5, 2014

HeartStart MRx Monitor/Defibrillator; Model(s), Catalogue, or Code Number: M3535A, M3536A, M3536J, M3536MC The…

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

Philips Medical Systems, Inc.

6 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Mar 5, 2014

Candy coated popcorn shaped into a heart weighing 1.5 ounces per piece and individually wrapped in clear plastic…

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

Popcorn Factory, The

FDA (openFDA food enforcement)

Medical devices

Reported Mar 5, 2014

pCO2 D788 Membranes. Distributed by Radiometer America, Inc., Westlake, OH. An automatic or semi-automatic instrument…

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

Radiometer America Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 5, 2014

Reflection Interfit Shell, 52 MM OD, 3 HOLE, REF 71336052, QTY 1, STERILE R, Smith & Nephew, Inc. Indications for use…

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

Smith & Nephew Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 5, 2014

VirtuoSaph¿ Plus Endoscopic Vessel Harvesting System, Part number: VSP550, Sterile***Rx Only*** Product Usage: The…

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

Terumo Cardiovascular Systems Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Mar 5, 2014

PREMIER CARE RECLINER 5570 with Urethane armrests, Multiple side-table options, 3 position lock-bar, Fully upholstered,…

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

Winco Mfg., LLC

3 more products in this recall

FDA (openFDA device enforcement)

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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.