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 Oct 2, 2019
APS Accelerator modular systems, 208-230 V-, 50/60 Hz, 1800 VA, IVD, RX, Class 2 Laser Product,
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Laboratories, Inc.
FDA (openFDA device enforcement)
Reported Oct 2, 2019
Udi's Classic Hamburger Buns, packaged in a 10.4 oz. plastic bag, with eight bags per wholesale case. UPC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ConAgra Foods, Inc.
FDA (openFDA food enforcement)
Reported Oct 2, 2019
The HEMASHIELD PLATINUM Woven Double Velour Vascular Graft is a woven double velour polyester graft impregnated with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Getinge US Sales LLC
FDA (openFDA device enforcement)
Reported Oct 2, 2019
Gold Cup Leadwire and Snap Leadwire with the following component descriptions: 1. 24" Snap Leadwire, Blue; 2. 40" Snap…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GN Otometrics
FDA (openFDA device enforcement)
Reported Oct 2, 2019
Philips HeartStart Infant/Child SMART Pads Cartridge, Model # M5072A, UDI:00884838023758
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips North America LLC
FDA (openFDA device enforcement)
Reported Oct 2, 2019
Medfusion¿ Model 4000 Syringe Infusion Pump, with PharmGuard¿ Server Software (PGS). Sold under the following names:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD Inc.
FDA (openFDA device enforcement)
Reported Sep 25, 2019
Subcutaneous Implantable Cardioverter Defibrillator (S-ICD) System, labeled as EMBLEMTM S-ICD Pulse Generator
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 25, 2019
LEEP Return Patient Pads (10/ box) Model # 6050Pl used in electrosurgical procedures.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.CooperSurgical, Inc.
FDA (openFDA device enforcement)
Reported Sep 25, 2019
MiCal brand YELLOWFIN TUNA POKE CUBE, Raw, Frozen, Product of Vietnam, Wild Caught. Cube size - 1 inch (2cm x 2cm) AAA…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stavis Seafoods, Inc.
FDA (openFDA food enforcement)
Reported Sep 25, 2019
Hemospray Endoscopic Hemostat
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Wilson-Cook Medical Inc.
FDA (openFDA device enforcement)
Reported Sep 18, 2019
Natrelle, Saline-Filled Breast Implant Biocell Full Height with Fill Tube, Sterile, for the following style numbers:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Allergan PLC
14 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 18, 2019
YoCrunch VANILLA LOWFAT YOGURT WITH SNICKERS PIECES 4 - 4 oz (113g) - 16 oz (453g) 6 packaged or 4 cups per case. UPC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Danone Waters
FDA (openFDA food enforcement)
Reported Sep 18, 2019
Martha White Gluten Free Sweet Yellow Cornbread & Muffin Mix packaged in a 7oz. pouch. 12 pouches per wholesale case.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hometown Food Company
FDA (openFDA food enforcement)
Reported Sep 18, 2019
Plastic Bottles labeled with: "Ancient Youth Secret - Since 500 B.C., DR. NARAM'S RASAYANA D TABLET, Calcium Supplement…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Jivan Shakti Inc.
FDA (openFDA food enforcement)
Reported Sep 18, 2019
PediaSmart Organic Soy Vanilla Beverage Mix, 12.7 oz. (360g) composite can
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Natures One Inc.
FDA (openFDA food enforcement)
Reported Sep 18, 2019
Stonyfield Kids Strawberry Beet Berry Tubes, 8 count-2oz each; 453g/package; Keep Refrigerated
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stonyfield Farm
FDA (openFDA food enforcement)
Reported Sep 18, 2019
Dynex DSX Software-IVD ELISA Assays effected as follows: DSX Assay File Software: ZEUS vl B. burgdorferi lgG-lgM.asy…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zeus Scientific, Inc.
FDA (openFDA device enforcement)
Reported Sep 18, 2019
XP- CR Tibial Tray- Interlok 59mm Item # 195268
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
34 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 11, 2019
Alere Cholestech LDX Analyzer, model # 14-874 containing power supplies with the identifying codes of 1837d and 1843d -…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alere San Diego, Inc.
FDA (openFDA device enforcement)
Reported Sep 11, 2019
AngioDynamics VenaCure EVLT NeverTouch Procedure Kit, 45CM NEVERTOUCH FRS .018 PROCEDURE KIT PG, Catalog Number 11403012
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Angiodynamics, Inc.
FDA (openFDA device enforcement)
Reported Sep 11, 2019
Norm-O-Temp model 111Z
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cincinnati Sub-Zero Products LLC, a Gentherm Company
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 11, 2019
Berchtold Chromophare Dual Monitor Carrier Arm or Dual Flat Panel, a component of Berchtold Chromophare Ceiling Mounted…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Communications
FDA (openFDA device enforcement)
Reported Sep 4, 2019
EQUISTREAM LONG-TERM HEMODIALYSIS CATHETER, REF/Product Code:5905190, 14.5 Fr. Alphacurve Catheter with Standard Kit,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
27 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 4, 2019
All colors and sizes of Confectionery Arts International, LLC brand Jewel Dust, a pearlescent pigment, manufactured and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Confectionery Arts International, LLC
FDA (openFDA food 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.