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 Mar 30, 2016
Toshiba DRAD-3000E FPD Wireless System Product Usage The DRAD-3000¿ is intended for use with the ceiling-suspended tube…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Toshiba American Medical Systems Inc.
FDA (openFDA device enforcement)
Reported Mar 30, 2016
ShopRite Dry Roasted Unsalted Cashews 7 oz. (198 g) Distributed by Wakefern Food Corp., Elizabeth, NJ 07207 UPC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Wakefern Foods Corp.
FDA (openFDA food enforcement)
Reported Mar 23, 2016
CORDIS AVANTI + CATHETER SHEATH INTRODUCER SYSTEM The product includes a Catheter Sheath Introducer (CSI) and a vessel…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cordis Corporation
FDA (openFDA device enforcement)
Reported Mar 23, 2016
McKesson Horizon Medical Imaging (HMI) products versions 4.6.1 to including 11.9 and McKesson Radiology (MR) products…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mckesson Medical Immaging
FDA (openFDA device enforcement)
Reported Mar 23, 2016
Accu-Chek Inform II Base Unit as a part of the Accu-Chek Inform II Blood Glucose Monitoring System Accu-Chek inform II…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Operations, Inc.
FDA (openFDA device enforcement)
Reported Mar 23, 2016
Siemens Syngo Dynamics-a Picture Archiving and Communication System (PACS) Model Numbers: 10091805, 10091807, 10091637,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Mar 16, 2016
Super Arrow-Flex Percutaneous Sheath Introducer Sets REF CL-07035 or CL-07635 or CL-07735 or CL-07835 Super Arrow-Flex…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arrow International Inc.
FDA (openFDA device enforcement)
Reported Mar 16, 2016
Denali Filter-Jugular/Subclavian Delivery System Product Code: DL900J/DL950J; Indicated for use in the prevention of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 16, 2016
IMPAK ACRYLIC RESIN LIQUID FOR BOTH IMPAK & IMPAK-PF POWDERS 1 qt. size (946 cc), Part Number 3306, and 11 oz. size…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CMP Industries, LLC
FDA (openFDA device enforcement)
Reported Mar 16, 2016
Large Volume Paracentesis Kit is packaged in a thermaformed tray which contains slots and snap-in holders for most…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Gi Supply
FDA (openFDA device enforcement)
Reported Mar 16, 2016
Philips X-Ray Systems, Allura Xper with R8.2.16 Product Usage: The Allura Xper FD1O and Allura Xper FD1O/10 is intended…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Electronics North America Corporation
FDA (openFDA device enforcement)
Reported Mar 16, 2016
Clasen Quality Coatings NH Atlas 1M Creamy Peanut Drop, Item # 12649, Net Wt. 50 lbs (22.68 KG)
High riskUsing this product could cause serious injury, illness or death — stop using it now.R&D Technical Center
FDA (openFDA food enforcement)
Reported Mar 16, 2016
Spacelabs Healthcare Xhibit Central Station, Model 96102 is used to provide clinicians with central monitoring of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spacelabs Healthcare Inc.
FDA (openFDA device enforcement)
Reported Mar 16, 2016
Heartland Flax Meal, Net Wt. 50 lbs.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Specialty Commodities, Inc.
FDA (openFDA food enforcement)
Reported Mar 16, 2016
ROTROL P Control for ROTEM delta Thromboelastometry System, For In Vitro Diagnostic Use Only. Quality control material…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.TEM Systems Inc.
FDA (openFDA device enforcement)
Reported Mar 9, 2016
Braga Organic Farms Organic Pistachio Kernels, Raw; Certified Organic, USDA Organic. Packed in 8 oz. 1 lb. 2. lb and 5…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Braga Organic Farms, Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Mar 9, 2016
Nebulizer Masks Opti-Mist and Opti-Mist Clear Nebulizer masks are intended to spray liquids in aerosol form into gasses…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ConvaTec, Inc.
FDA (openFDA device enforcement)
Reported Mar 9, 2016
Restoris Multicompartmental Knee (MCK) System RESTORIS MCK is indicated for single or multi-compartmental knee…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mako Surgical Corporation
FDA (openFDA device enforcement)
Reported Mar 9, 2016
Medtronic Custom Perfusion Tubing Pack, Rx, Sterile EO. Terumo Cardiovascular Systems (Terumo CVS) has distributed an…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Medtronic Perfusion Systems
FDA (openFDA device enforcement)
Reported Mar 9, 2016
BrightView are gamma cameras; Designed for single or dual detector nuclear imaging.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 2, 2016
BD FMC7 FITC: Model 430918. FMC7 is intended for in vitro diagnostic use in the identification of cells expressing FMC7…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Becton, Dickinson and Company, BD Biosciences
FDA (openFDA device enforcement)
Reported Mar 2, 2016
HipLOC CHS Plate/Lag Screw Introducer
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet, Inc.
FDA (openFDA device enforcement)
Reported Mar 2, 2016
Hill-Rom Bariatric Power Recliner, Product Model # P9096 Hill-Roms 660 lb Powered Bariatric Recliner was created to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hill-Rom, Inc.
FDA (openFDA device enforcement)
Reported Mar 2, 2016
This reagent is for in vitro diagnostic use. Pax-5 (1EW) monoclonal antibody is intended to be used for the qualitative…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Leica Microsystems, 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.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.
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.