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.
4,822 stored notices name New Jersey, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,784 notices were distributed nationwide, so they reach New Jersey too — those are in the archive.
Reported Jan 22, 2020
Butler's Dark Chocolate with Irish Whisky, 3.52oz bar, UPC 8 44984 17619 7, 10 units per case
High riskUsing this product could cause serious injury, illness or death — stop using it now.Gourmet International Ltd.
FDA (openFDA food enforcement)
Reported Jan 22, 2020
LIFEPAK 15 MONITOR/DEFIBRILLATOR that was either manufactured with or received an upgrade kit that contained an…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Physio-Control, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 22, 2020
Stop and Shop brand Grilled Salmon meal with cooked brown rice, quinoa blend, broccoli florets, cooked white rice, fire…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Taylor Farms New England, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jan 22, 2020
Teleflex MEDICAL RuSCH One piece Male External Regular Catheter W/O Tape, REF A1500
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Teleflex Medical
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 22, 2020
Signature Crab Cake, Signature Crab Cake (2 pk), and Signature Crab Cake (4pk); Wegmans Ready to Cook Signature Crab…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Wegmans Food Markets, Inc.
21 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 15, 2020
ImplantDirect InterActive Precision IO Scan Adapter, Part #6534-09PT, Platform: 3.4mm, Non-Sterile, Rx. The firm name…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Implant Direct Sybron Manufacturing, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 15, 2020
Medacta Shoulder SYSTEM HUMERAL ANATOMICAL METAPHYSIS, REF 04.01.0023 through 04.01.0055, all sizes - Product Usage:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medacta USA Inc.
FDA (openFDA device enforcement)
Reported Jan 15, 2020
NANCY ADAMS DARK CHOCOLATE Graham Crackers, NET WT 7.5 OZ (212G); UPC 618645275860; packaged in a brown paper bag with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nassau Candy Distributors, Inc.
FDA (openFDA food enforcement)
Reported Jan 15, 2020
Cios Alpha, Model Number 10308191; mobile X-Ray system designed to provide X-ray imaging of the anatomical structures…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Jan 15, 2020
GREY GHOST BAKERY scratch-made cookies LEMON SUGAR NET WT 1.4 OZ (40 G), UPC 8 53152 00308 1 , 4 OZ (113 G) UPC 8 53152…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.TFI Holding dba Grey Ghost Bakery
FDA (openFDA food enforcement)
Reported Jan 8, 2020
Classic Lays potato chips 2 3/4 oz. UPC 28400 42054; Classic Lays potato chips 8 oz. UPC 28400 19914; Classic Lays…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Frito-Lay, Inc.
FDA (openFDA food enforcement)
Reported Jan 8, 2020
RANITIDINE TABLETS, USP 150mg, 10,000-count bag, Country of Origin: INDIA NDC 62207-773-32
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Granules India Limited
FDA (openFDA drug enforcement)
Reported Jan 8, 2020
NIDEK Specular Microscope, Model CEM-530 - Product Usage: The device provides noncontact, high magnification image…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Nidek, Inc.
FDA (openFDA device enforcement)
Reported Jan 8, 2020
HeartMate 3 Mobile Power Unit, REF 107754, UDI or GTIN: 00813024010883, and 107758, UDI or GTIN: 00813024010890, when…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Thoratec Corp.
FDA (openFDA device enforcement)
Reported Jan 8, 2020
Juno DRF, Model Number 709020 - Product Usage: General. multi-function x-ray systems capable of routine radiographs and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Villa Sistemi Medicali S.P.A.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 3, 2020
Kettle Cuisine Midco, LLC, Recalls Ready-To-Eat Soup Products due to Misbranding and Undeclared Allergens
High riskUsing this product could cause serious injury, illness or death — stop using it now.Kettle Cuisine Midco, LLC
USDA FSIS
Reported Jan 1, 2020
STA UNICALIBRATOR (ref. 00675)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Diagnostica Stago, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 1, 2020
R.H. Macys & Co. Roasted Salted Cherries Berries and Nuts with Dark Chocolate, in 10oz metal tin, UPC - 788709600362
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ferris Coffee and Nut Company, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jan 1, 2020
Trader Joe's 8pcs Spicy California Roll, 8oz, SKU 00348966T
High riskUsing this product could cause serious injury, illness or death — stop using it now.Fuji Food Products, Inc.
22 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 1, 2020
VNS Therapy, SenTiva, Model # 1000, (01)05425025750405, Rx Only for vagal nerve stimulation (VNS) therapy
High riskUsing this product could cause serious injury, illness or death — stop using it now.LivaNova USA Inc.
FDA (openFDA device enforcement)
Reported Jan 1, 2020
PTS Panels CHOL+HDL+GLU Test Strips, Reference Number 5412, for use on CardioChek PA or CardioChek Plus analyzers
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Polymer Technology Systems, Inc.
FDA (openFDA device enforcement)
Reported Jan 1, 2020
RayStation stand-alone software treatment planning system, Model Numbers 4.0, 4.5, 4.7, 4.9, 5.0, 6.0, 6.1, 6.2, 6.3,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Raysearch Laboratories Ab
FDA (openFDA device enforcement)
Reported Dec 25, 2019
Natrelle Saline-Filled Breast Implant, for the following Styles and sizes, Style LP, Style 68 HP, Style 68 MP, Style…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Allergan PLC
3 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 25, 2019
Alliance Tech Medical, Inc. All Flow Pulmonary Function Filters, 100 filters individually packaged in a clear, sealed…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alliance Tech Medical, Inc.
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.