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.
Reported Dec 14, 2016
BON APPETITO WALNUT LADIES FINGER, Net Wt.: 10oz. (340g), UPC 6 44744 69876 7
High riskUsing this product could cause serious injury, illness or death — stop using it now.Golden Star International Inc.
FDA (openFDA food enforcement)
Reported Dec 14, 2016
Halyard C-Section Drape with Clear Screen and Full Incise (Non-Sterile), Product Code 44965 NS; C-Section Drape with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Halyard Health, Inc.
FDA (openFDA device enforcement)
Reported Dec 14, 2016
McConnell's Fine Ice Cream Dutchman's Chocolate
High riskUsing this product could cause serious injury, illness or death — stop using it now.McConnell's Ice Cream, Inc.
6 more products in this recall
FDA (openFDA food enforcement)
Reported Dec 14, 2016
Premium Norwegian Salmon, Smoked, slice 8oz (227g), UPC # 856687004288, Keep refrigerated
High riskUsing this product could cause serious injury, illness or death — stop using it now.Olma-Xxi Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Dec 14, 2016
Olympus Scientific Solutions Americas Corporation ( OSSA ) Model: VANTA Analytical X-Ray System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Olympus Scientific Solutions Americas
FDA (openFDA device enforcement)
Reported Dec 14, 2016
Airheads Mini Bars 12oz bags of assorted flavors. 12 - 12oz bags are included in cardboard cartons. Assorted flavors…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Perfetti Van Melle USA Inc.
FDA (openFDA food enforcement)
Reported Dec 14, 2016
Brilliance 64 728231 Computed Tomography X-ray systems intended to produce cross-sectional images of the body by…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 14, 2016
Radiation Therapy Treatment Planning System Product Usage: RayStation is a software system designed for treatment…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Raysearch Laboratories Ab
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 14, 2016
MOZZARELLA LOW MOISTURE WHOLE MILK 8/6# ARREZZIO IMPERIAL; UPC: 0 74865 30185 5 Saputo code: #101379 ;
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Saputo Cheese USA, Inc.
13 more products in this recall
FDA (openFDA food enforcement)
Reported Dec 14, 2016
ADVIA 560 Hematology Systems, Siemens Material Number (SMN) 11170842, IVD.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Dec 14, 2016
Perceval Sutureless Aortic Heart Valve size S, Item # ICV1208, REF PVS21; Perceval Sutureless Aortic Heart Valve size…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sorin Group USA, Inc.
FDA (openFDA device enforcement)
Reported Dec 7, 2016
Greatbatch, Offset Cup Impactor with the following Parts and Catalogue #: Tl0600 ~ MMP3100CHA04 T10491 MIMP3100CHA04…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Greatbatch Medical
FDA (openFDA device enforcement)
Reported Dec 7, 2016
MSS CASSETTE GLU/LAC/UREA (BUN) as a part of the Roche OMNI S Analyzer: cobas b 221<6>Roche OMNI S6 system The Roche…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Operations, Inc.
FDA (openFDA device enforcement)
Reported Nov 30, 2016
COBRA Fusion 50 Ablation System, COBRA Fusion 150 Ablation System, and COBRA Fusion Magnetic Retriever System. Model…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.AtriCure, Inc.
FDA (openFDA device enforcement)
Reported Nov 30, 2016
Enlightened Peanut Butter Chocolate Chip Ice Cream, one pint
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Cedar Crest Specialties, Inc.
FDA (openFDA food enforcement)
Reported Nov 30, 2016
The Hemotherm 400CE 115v, containing power board p/n 39945
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cincinnati Sub-Zero Products Inc.
FDA (openFDA device enforcement)
Reported Nov 30, 2016
BM Westco Mster Mix Raised Donut Mix, 50#
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CSM Bakery Products NA
21 more products in this recall
FDA (openFDA food enforcement)
Reported Nov 30, 2016
LIAISON Estradiol II Gen, 310680, 310680-CN The DiaSorin LIAISON Estradiol II Gen assay is a chemiluminescent…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Diasorin Inc.
FDA (openFDA device enforcement)
Reported Nov 30, 2016
Philips Healthcare System X-ray Tomography Computed :
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Electronics North America Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 30, 2016
KENALOG (Triamcinolone Acetonide) Spray with Spray Tube Topical Aerosol, USP, (0.147 mg/g), 15 g bottle, Physician…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Sun Pharmaceutical Industries, Inc.
FDA (openFDA drug enforcement)
Reported Nov 23, 2016
Access Ostase Calibrators, Catalog No. 37305, B83876 Product Usage: The Access Ostase Calibrators are intended to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 23, 2016
MEVION S250 Product Usage: Proton Radiation Therapy
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mevion Medical Systems, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 23, 2016
Version 1.2.0 of Accu-Chek Connect Diabetes Management App (iOS) released on July 11, 2016
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diabetes Care, Inc.
FDA (openFDA device enforcement)
Reported Nov 23, 2016
RF MultiGen¿, 0406-900-000; Refurb RF MultiGen¿, 0406-900-000U
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Stryker Instruments Div.
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.