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 48,122 notices were distributed nationwide, so they reach New Jersey too — those are in the archive.

Medical devices

Reported Apr 19, 2017

Keystone Dental Inc. PrimaConnex Straight Implant TC, WD Internal Connection 5.0 x 11.5mm. Catalog Number(s): 15636K

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

Keystone Dental Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 19, 2017

Nordson Micromedics FibriJet Endoscopic Catheter Introducer, Catalog Number SA-3445. Sterilized using Ethylene Oxide

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

Micromedics, Inc.

FDA (openFDA device enforcement)

Food

Reported Apr 19, 2017

LIDIA'S MARINARA, NET WT 25 oz (708g), UPC 897712001018 --- Manufactured for Nonna Foods LLC Woodbury, NY 11797

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

Nonna Foods

FDA (openFDA food enforcement)

Drugs

Reported Apr 19, 2017

Estradiol Micronized Bulk, Rx only, For Prescription Compounding, Manufactured by Qinhuangdao Zizhu Pharmaceutical Co.,…

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

Qinhuangdao Zizhu Pharmaceutical, Co.

6 more products in this recall

FDA (openFDA drug enforcement)

Medical devices

Reported Apr 19, 2017

Radiation Therapy Treatment Planning System, Model 4.5, 4.7, 5.0 RayStation is a software system designed for treatment…

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

Raysearch Laboratories Ab

FDA (openFDA device enforcement)

Medical devices

Reported Apr 19, 2017

Cobas 8100 bi-directional reformatter (BRF) module with Software Version 02-xx

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

Roche Diagnostics Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 19, 2017

CADD¿ Administration Set, 21-7339-24, Rx Only, Sterile EO.

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

Smiths Medical ASD Inc.

FDA (openFDA device enforcement)

Food

Reported Apr 19, 2017

Vulto Creamery Ouleout soft wash-rind raw milk cheese cut and wrapped in clear plastic

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

Whole Foods Market

4 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Apr 19, 2017

Cataract Kit, part numbers CAT1467AM and CAT1538(B. Product packaged in a convenient manner for use in a general…

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

Windstone Medical Packaging, Inc.

17 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 12, 2017

DX-D600 - DXD Imaging Package

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

AGFA Healthcare Corp.

FDA (openFDA device enforcement)

Food

Reported Apr 12, 2017

DELALLO Premium Sliced COLBY CHEESE NET WT. 8 OZ. (227G) INGREDIENTS: Cultured Pasteurized Milk, Salt, Enzymes, Annatto…

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

Biery Cheese, Inc.

13 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Apr 12, 2017

POST-OP EYE TRAY The Covidien Curity Oval Eye Pads are individually packaged and sterilized by the manufacturer; they…

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

Centurion Medical Products Corporation

6 more products in this recall

FDA (openFDA device enforcement)

Drugs

Reported Apr 12, 2017

Cotellic (cobimetinib) Tablets, 20 mg, 63 count bottle, Rx Only, Made in Switzerland. Distributed by Genentech USA,…

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

Genentech Inc.

FDA (openFDA drug enforcement)

Food

Reported Apr 12, 2017

Dark Chocolate bars Choklad Mork Dark Chocolate, Net Wt. 3.5 OZ. AND Chokland Mork Dark Chocolate 70%, Net Wt. 3.5 OZ.…

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

Ikea North America Srvcs Inc.

5 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Apr 12, 2017

BrightView SPECT model number 882480 BrightView and BrightView X are gamma cameras designed for single or dual detector…

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

Philips Medical Systems (Cleveland) Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 5, 2017

AGFA Digital Radiography X-Ray System DX-D100 DX-D100 is indicated for use in providing diagnostic quality images to…

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

AGFA Healthcare Corp.

FDA (openFDA device enforcement)

Food

Reported Apr 5, 2017

Baidyanath brand Sarivadi Bati, Dietary Supplement, 80 Tablets -- Product of India --- Mfd in India - Shree Baidyanath…

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

Butala Emporium, Inc.

9 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Apr 5, 2017

JResultNet drivers using ASTM coding language. Calculator/data processing module, for clinical use - Stand-alone…

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

Data Innovations, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Apr 5, 2017

Legionella IFA (IF0950) intended for qualitatively detecting and semi-quantitating human serum antibodies to Legionella…

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

Focus Diagnostics Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 29, 2017

Hitachi Oasis MRI System

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

Hitachi Medical Systems America Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 29, 2017

Brilliance BigBore Oncology CT - 728243 Computed Tomography X-ray systems intended to produce cross-sectional Images of…

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

Philips Medical Systems (Cleveland) Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 29, 2017

Raindrop Near Vision Inlay, Model# RD1-1

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

Revision Optics Inc.

FDA (openFDA device enforcement)

Food

Reported Mar 29, 2017

Sargento Ultra Thin Sliced Longhorn Colby, 6.84 oz., UPC 4610000228, with Sell By dates of 12APR17B, 02FEB17F,…

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

Sargento Foods, Inc.

16 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Mar 29, 2017

Arial Wireless Water-Resistant Call Pendant The Arial Pendant tag is part of the Arial wireless emergency call…

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

Stanley Security Solutions Inc.

FDA (openFDA device enforcement)

Free recall alerts

Get alerted about new New Jersey recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

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.