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.
Reported Feb 3, 2016
Vantage Panoramic X-Ray System used to perform dental and orthodontic radiological imaging The Vantage Panoramic X-Ray…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Midmark Corp. dba Progeny Inc.
FDA (openFDA device enforcement)
Reported Feb 3, 2016
EliA SmDP Well, Article Number 14-5624-01 Product Usage: EliA SmDP is intended for the in vitro semi-quantitative…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Phadia Ab
FDA (openFDA device enforcement)
Reported Jan 27, 2016
TLC¿ Self Retaining Retractor System Contents 1-RETRACTOR FRAME 6-ELASTIC STAYS STERILE EO Rx ONLY. Indicated for use…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abeon Medical Corporation
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 25, 2016
Berks Packing Co. Recalls Beef Products Due to Misbranding
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Berks Packing Co., Inc.
USDA FSIS
Reported Jan 25, 2016
Whole Foods Recalls Frozen Pizza Products Due to Misbranding
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Whole Foods
USDA FSIS
Reported Jan 20, 2016
NIPRO SET / SLIMLINE BLOOD TUBING SET for Hemodialysis with Transducer Protectors and Priming Set A disposable…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nipro Medical Corporation
FDA (openFDA device enforcement)
Reported Jan 20, 2016
UniAxial Pedicle Screw & UniAxial Reduction Pedicle Screw The Response 5.5/6.0 Spine System is intended for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.OrthoPediatrics Corp.
FDA (openFDA device enforcement)
Reported Jan 20, 2016
Ergon 2 Articulating Equipment Boom Monitor Brackets mounting point for display interfaces utilized in clinical…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Skytron, Div. The KMW Group, Inc.
FDA (openFDA device enforcement)
Reported Jan 20, 2016
TWININGS OF London ENGLISH BREAKFAST BLACK TEA DECAFFEINATED, 12-0.11OZ (3.2g)/ EA NET WT 1.34 oz (38g), UPC…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Twinings North America, Inc.
FDA (openFDA food enforcement)
Reported Jan 20, 2016
Zimmer, Virage OCT Spinal Fixation System, Item Number: 07.01738.001, a posterior system intended to achieve an implant…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 13, 2016
Natus Quantum System with NeuroWorks Software. Catalog /Part Numbers: 013926. The Natus Quantum Amplifier is intended…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Natus Neurology dba Excel Tech., Ltd. (XLTEK)
FDA (openFDA device enforcement)
Reported Jan 13, 2016
Nicomex Velitas Candies Candles Net. Wt. 2 oz (56.7 gms) Distributed by Nicomex Inc. 88 First Street, Passaic, NJ 07055
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nicomex Inc.
FDA (openFDA food enforcement)
Reported Jan 13, 2016
Remote Patient Monitoring System, MDP 2000 Series, Part Numbers: MDP2040-0100, PGM340R3, or PGM340R4. The MDP2000 is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vidco, Inc.
FDA (openFDA device enforcement)
Reported Jan 6, 2016
Barilla MEDIUM SHELLS, 1 LB (454 g), GTIN 00076808002881, packed as twelve boxes in 1 case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Barilla America NY, Inc.
3 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 6, 2016
MOSAIQ Oncology Information System MOSAIQ is an oncology information system used to manage workflows for treatment…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Jan 6, 2016
Simply Enjoy Shrimp and Lobster Ravioli, 9 oz, refrigerated packaged in plastic tray. Distributed by Foodhold USA,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nuovo Pasta Productions, Ltd.
FDA (openFDA food enforcement)
Reported Jan 6, 2016
Ceiling Mounted Surgical Light System TruLight 3000/5000 and Ceiling Mounted Surgical Light System iLED3/iLED5
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Trumpf Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Jan 5, 2016
Wegmans Food Markets Retira Productos De Pollo Producidos Sin El Beneficio De Una Inspeccin Federal
High riskUsing this product could cause serious injury, illness or death — stop using it now.Wegmans Food Markets
USDA FSIS
Reported Dec 30, 2015
Vancomycin Screen Agar
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)
Reported Dec 30, 2015
Etest¿ Piperacillin/tazobactam (4 ug/mL) PTc0.016-256-pack of 30 tests WW Etest¿ is a quantitative technique for…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Biomerieux
3 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 30, 2015
A.L.P.S. 4.0mm Cancellous Locking Screws intended for use in stabilization and fixation of fractures, revision…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 30, 2015
Boston Scientific, Chariot ST-CCV Guiding Sheath, Sterilized using ethylene oxide: Product Description Material Number…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Boston Scientific Corporation
FDA (openFDA device enforcement)
Reported Dec 30, 2015
VAPR¿ TRIPOLAR 90" Degree Suction Electrodes (Model/Catalog No: 225028)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Mitek, Inc., a Johnson & Johnson Co.
FDA (openFDA device enforcement)
Reported Dec 30, 2015
Optional PS500 Power Supply Unit for the Evita V500 Ventilator and Babylog VN500 Ventilator. Babylog VN500 is a…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Draeger 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.