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 May 8, 2019
Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 6), product code 35700BAX - Product Usage: The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
FDA (openFDA device enforcement)
Reported May 8, 2019
FilmArray Gastrointestinal (GI) Panel, IVD, Rx Only, Biofire Diagnostics, LLC REF: RFIT-ASY-0104, and RFIT-ASY-0116),…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioFire Diagnostics, LLC
FDA (openFDA device enforcement)
Reported May 8, 2019
CAROLINA(R) LIQUID CHEMISTRIES CORP. ETHA RGT. KIT, IVD, REF ST321
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Carolina Liquid Chemistries
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 8, 2019
Harmless Harvest Dairy-Free Yogurt Drink; Cultured Coconut Drink; Probiotic Original Unsweetened. 8 fl. oz. plastic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Harmless Harvest Inc.
3 more products in this recall
FDA (openFDA food enforcement)
Reported May 8, 2019
Lamb s Supreme Potato Tater Puffs, item # H30, packaged in 5-pound unprinted KRAFT paper bags, 6 bags to a case, sold…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lamb Weston BSW LLC
FDA (openFDA food enforcement)
Reported May 8, 2019
EZ Derm Porcine Xenograft, labeled as the following: a. EZ Derm 3x4 (8x10 cm) Non-Perforated, Part Number: 131703-03;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Molnlycke Health Care, Inc.
FDA (openFDA device enforcement)
Reported May 8, 2019
cobas e 801 immunoassay analyzer
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Corporation
FDA (openFDA device enforcement)
Reported May 1, 2019
St. Jude Medical Confirm Rx Insertable Cardiac Monitor, REF DM3500, Sterile. Product Usage: The St. Jude Medical…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott
FDA (openFDA device enforcement)
Reported May 1, 2019
RT Elements Software revisions of the RT Elements applications have a specific software version number. Specifically…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Brainlab AG
FDA (openFDA device enforcement)
Reported May 1, 2019
Truliant Tibial Fit Tray Cemented SZ 3F / 3T, Catalog Number 02-022-45-3030 Product Usage: Knee joint…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Exactech, Inc.
FDA (openFDA device enforcement)
Reported May 1, 2019
Fresenius Kabi CATSmart device (Continuous autotransfusion System). Labeled as the following kits: 1. AT-1 sets and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fenwal Inc.
FDA (openFDA device enforcement)
Reported Apr 24, 2019
FilmArray BCID Panel, IVD, Rx Only, BioFire Diagnostics, REF: RFIT-ASY-0126, and RFIT-ASY-0127, when used with the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioFire Diagnostics, LLC
FDA (openFDA device enforcement)
Reported Apr 24, 2019
BIOVENTUS Bioactive Bone Graft Putty 15g Rx only/sterile. Filler device intended for use in bony voids or gaps that are…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bioventus, LLC
FDA (openFDA device enforcement)
Reported Apr 24, 2019
Cordis Vista Brite Tip & Androit Guiding Catheters Product Usage: The guiding catheter is intended for use for…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Cordis Corporation
FDA (openFDA device enforcement)
Reported Apr 24, 2019
Salto Talaris, Tibial Total Ankle Prosthesis Tray, Talar Dome, Size 0, Right, Part No. LJU200T
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corp.
25 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 24, 2019
14F SLX Double Lumen Full Tray Hemodialysis catheter insertion kits, Item No. MC061422
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medical Components, Inc. dba MedComp
FDA (openFDA device enforcement)
Reported Apr 24, 2019
ProSun Onyx 32 Sli Intensive (12 minutes) tanning bed, Model 32/1. Labeled as the following: PROSUN ONYX 32 SLI…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ProSun International, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 24, 2019
Acusnare Polypectomy (Duck Bill Shaped) Snare Used with an electrosurgical unit for endoscopic polypectomy.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Wilson-Cook Medical Inc.
FDA (openFDA device enforcement)
Reported Apr 17, 2019
CORAIL AMT STANDARD OFFSET NECK SEGMENT (STD), Pro. Code L20431 Product Usage: The affected CORAIL Neck Trials are…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Orthopaedics, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 17, 2019
Commercial Breader Batter; A28177 BATTER MIX X1; 50 pound bag
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Newly Weds Foods Inc.
30 more products in this recall
FDA (openFDA food enforcement)
Reported Apr 17, 2019
syngo.via syngo.CT Cardiac Function, Model Number 10496180 Product Usage: Syngo.CT Cardiac Planning and syngo CT.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 10, 2019
The UniCel DxI 600 and 800 Access Immunoassay Systems, that are connected to an automation line. UniCel DxI 600 Catalog…
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 Apr 10, 2019
McKesson Consult Diagnostic Immunochemical Fecal Occult Blood Test, Part numbers 178-CK30T, 178-CT30, 178¿TBSO,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Cypress Medical Products LLC
FDA (openFDA device enforcement)
Reported Apr 3, 2019
BVI Visitec Soft Tip Cannula, 0.8MM .50 x 33mm (25G x 1.3 in). The BVI Soft Tip Cannula is intended to irrigate and/or…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beaver Visitec
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.