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 Sep 8, 2021
Artis Models with SW version VD12 listed below: Artis zee floor 10094135 Artis zee ceiling 10094137 Artis zee MP…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Sep 8, 2021
CareStart COVID-19 Antigen Rapid Diagnostic Test for the detection of SARS-CoV-2 Antigen Qualitative detection of the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Versea Diagnostics LLC
3 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 8, 2021
CoolSculpting Elite System The CoolSculpting System SW release 2.0, SW release 3.0, SW release 3.0.1, SW release 3.0.2
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zeltiq Aesthetics, Inc.
FDA (openFDA device enforcement)
Reported Sep 1, 2021
AUGMENT Injectable Kit, 3cc, Model K30003010, Lot 1706343
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioMimetic Therapeutics, LLC
FDA (openFDA device enforcement)
Reported Sep 1, 2021
Monoject 0.9% Sodium Chloride Flush Syringe, 10 mL Fill, STERILE, Product Code 8881570121 The proposed device is…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Cardinal Health
2 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 1, 2021
NES Reprocessed Visions PV .035 IVUS Catheter, Sterile. For use in the evaluation of vascular morphology in blood…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Northeast Scientific Inc.
FDA (openFDA device enforcement)
Reported Sep 1, 2021
AQUABEAM Handpiece, REF: HP2000, a sterile single-use component of the AQUABEAM Robotic System.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Procept Biorobotics Corporation
FDA (openFDA device enforcement)
Reported Sep 1, 2021
Gore Molding & Occlusion Balloon Catheter, REF Catalogue Number MOB37, SN XXXXXXXX, 10 mm - 37 m 10 Fr, Guidewire…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.W. L. Gore & Associates Inc.
FDA (openFDA device enforcement)
Reported Aug 25, 2021
Cell Marque Antibodies, PSA (ER-PR8) Mouse Monoclonal Antibody, REF: 324M-15, 324M-16
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Cell Marque Corporation
FDA (openFDA device enforcement)
Reported Aug 25, 2021
Triathlon Prim CEM FXD BPLT 7, Catalog No. 5520B700
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Howmedica Osteonics Corp.
FDA (openFDA device enforcement)
Reported Aug 25, 2021
OPTI SARS-CoV-2 RT-PCR Test, REF Numbers: a) 99-57003 b) 99-57004
Moderate riskThis product could cause temporary or reversible health problems — stop using it.OPTI Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Aug 25, 2021
CIRCUL8 LUXE DVT PREVENTION DEVICE, Aid in the Prevention of Deep Vein Thrombosis, REF: 08-0020, Rx Prescription Only,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho8, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 25, 2021
EPIQ Ultrasound Systems, Model: EPIQ Elite, EPIQ 5G, EPIQ 5C, EPIQ 5W, EPIQ 7G, EPIQ 7C, EPIQ 7W, EPIQ CVx, EPIQ CVxi
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Ultrasound Inc.
FDA (openFDA device enforcement)
Reported Aug 24, 2021
Willow Tree Poultry Farm Recalls Chicken Salad and Dip Products Due to Possible Foreign Matter Contamination
High riskUsing this product could cause serious injury, illness or death — stop using it now.Willow Tree Poultry Farm, Inc.
USDA FSIS
Reported Aug 18, 2021
ACCESS SARS-CoV-2 Antigen , REF: C68668, IVD, Rx only, UDI: (01) 15099590742713;
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 18, 2021
Kaluza C Flow Cytometry Software Versions: 1.0*, 1.1.1 and 1.1.2 Kits: C10574 - Kaluza C Single Perpetual License…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter, Inc.
FDA (openFDA device enforcement)
Reported Aug 18, 2021
FilmArray Blood Culture Identification (BCID) Panel Product Pouch Label: FilmArray BCID Panel Part No: RFIT-ASY-0126…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioFire Diagnostics, LLC
FDA (openFDA device enforcement)
Reported Aug 18, 2021
Alaris Infusion Pump Module, Model 8100, serviced/repaired by Biomedical Equipment Service Co. (BMES) with an impacted…
High riskUsing this product could cause serious injury, illness or death — stop using it now.BioMedical Equipment Service Co. (BMES)
FDA (openFDA device enforcement)
Reported Aug 18, 2021
ETEST IMIPENEM RELEBACTAM. in vitro diagnostic
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomerieux Inc.
FDA (openFDA device enforcement)
Reported Aug 18, 2021
Chassis Label - "CIRRUS HD-OCT Rx-Only" Product Label Exterior RX - "CIRRUS HD-OCT Model 6000"
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carl Zeiss Meditec, Inc.
FDA (openFDA device enforcement)
Reported Aug 18, 2021
Edwards PediaSat Oximetry Catheter Kit, REF: XT3515KTP, Exterior Diameter 5.5F (1.83 mm), Usable Length 15 cm, Number…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Edwards Lifesciences, LLC
5 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 18, 2021
Solumeve Hydrolyzed Collagen Peptides, Turmeric + MCT and Ginger; Dietary Supplement, NET Wt. 14.1 oz. (400g) Suggested…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Iherb LLC
FDA (openFDA food enforcement)
Reported Aug 18, 2021
McCormick Perfect Pinch Italian Seasoning 1.31 oz. Plastic Bottles, 36 packages per case; 2.25 oz. Plastic bottles, 6…
High riskUsing this product could cause serious injury, illness or death — stop using it now.McCormick & Company - MSS - HQ
2 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 18, 2021
Medtronic StimLoc Burr Hole Cover, Part Numbers: a) 3387S-40 b) 3389S-28 c) 3389S-40 d) 3391S-40 e) 3550S-01 f) 924256…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Neuromodulation
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.