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 Jul 16, 2014
Henora REF: 70-4026-09V1 300psi I.V. Catheter Extension Set Product Usage: Catheter extension set for high pressure…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.RGI Medical Manufacturing, Inc.
FDA (openFDA device enforcement)
Reported Jul 16, 2014
The STERIS 4085 General Surgical Table Product Usage: is an electro-hydraulically operated surgical table designed to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Steris Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 16, 2014
Terumo¿ Advanced Perfusion System 1 100/120V AC, Advanced Perfusion System Platform (APS)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 9, 2014
Atrium Express Dry Seal Chest Drain ATS Blood Recovery, Catalog Number: 4050-100N. Autotransfusion Apparatus.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Atrium Medical Corporation
FDA (openFDA device enforcement)
Reported Jul 9, 2014
Rosemary & Olive Oil Gluten Free Snack Crackers sold under the following brand names and sizes: 1. glutino, Net Wt.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Baptista's Bakery, Inc.
FDA (openFDA food enforcement)
Reported Jul 9, 2014
BD FACS Canto and associated Fluidics Cart Product Usage: Flow cytometer for use in In vitro Diagnostics.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BD Biosciences, Systems & Reagents
FDA (openFDA device enforcement)
Reported Jul 9, 2014
The Claymount Harmony is a grid cabinet designed to accept a digital x-ray imaging receptor and stationary grid. It…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Claymount Assembli
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 9, 2014
Stirling Ultracold Portable Shuttle, ULT-25. Storage for cold-chain management, short-term or long-term ultra-low and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Global Cooling Inc.
FDA (openFDA device enforcement)
Reported Jul 9, 2014
illumipro-10 Incubator/Reader, Meridian Bioscience, Inc. The illumipro-10 incubator/reader is designed to be used with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Meridian Bioscience Inc.
FDA (openFDA device enforcement)
Reported Jul 9, 2014
Kirkland Signature Coarse Ground Malabar Pepper, 12.7 oz Plastic Jars, UPC 096619164998. Packaging includes a PET…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Olde Thompson, Inc.
FDA (openFDA food enforcement)
Reported Jul 9, 2014
BrightView XCT: product code 882482, BrightView X- upgraded with the XCT Flat Panel Detector (FPD): product code…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
FDA (openFDA device enforcement)
Reported Jul 9, 2014
Siemens Mobilett XP Digital Mobile X-ray System Product Usage: The Mobilett XP and Mobilett XP Hybrid are radiographic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Jul 9, 2014
Stryker Orthopaedics Triathlon Tritanium Patella Inserter, . NON-STERILE Product Usage: The Triathlon Tritanium Patella…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Howmedica Osteonics Corp.
FDA (openFDA device enforcement)
Reported Jul 9, 2014
Anspach Pneumatic and Electric Motor Systems. Intended for cutting and shaping bone, including the spine and cranium.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Anspach Effort, Inc.
FDA (openFDA device enforcement)
Reported Jul 2, 2014
MOSAIQ MOSAIQ is an oncology information system used to manage workflows for treatment planning and delivery. It…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Jul 2, 2014
Glucose Hexokinase Liquid Reagent For the in vitro quantitative determination of Glucose in serum.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.JAS Diagnostics Inc.
FDA (openFDA device enforcement)
Reported Jul 2, 2014
Puritan Bennett 840 Ventilator (4-840120DIUU-XX) The PB840 Ventilator System is intended to provide invasive or…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nellcor Puritan Bennett Inc. (dba Covidien LP)
FDA (openFDA device enforcement)
Reported Jul 2, 2014
Brilliance CT Big Bore Oncology Whole Body Computed Tomography X-Ray System & Brilliance CT Big Bore Radiology Whole…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
FDA (openFDA device enforcement)
Reported Jul 2, 2014
Siemens StreamLAB(R) Analytical Workcell; Catalog number 746002.901. Designed to automate sample handling and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 2, 2014
Model RG3000 and RG4000 Series Valve Integrated Pressure Regulator (VIPR)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Western / Scott Fetzer Company
FDA (openFDA device enforcement)
Reported Jul 2, 2014
VerSys¿ Hip System, Beaded Fullcoat Stems, Zimmer, Inc., Warsaw, IN 46581
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, Inc.
FDA (openFDA device enforcement)
Reported Jun 27, 2014
Pennsylvania Firm Recalls Deli Ham Product Due To Possible Foreign Matter Contamination
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pennsylvania Firm
USDA FSIS
Reported Jun 25, 2014
Pacific Cod, skinless boneless fillet; vacuum packaged in a clear plastic bag. The wt of the fish is the only labeling…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kodiak Wild Alaska Seafood
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jun 25, 2014
Model Number(s): PB840 Ventilator (4-840120DIUU-XX). The product is a component of the Puritan Bennett 840 Ventilator:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nellcor Puritan Bennett Inc. (dba Covidien LP)
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.