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 Apr 27, 2022
Philips Respironics V60 Ventilator (All Models, including: 1053613, 1053614, 1053615, 1053616, 1053617, 1053618,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Respironics California, LLC
2 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 27, 2022
Merlin PCS 3650 programmer Model 3330 software
Moderate riskThis product could cause temporary or reversible health problems — stop using it.St. Jude Medical, Cardiac Rhythm Management Division
4 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 20, 2022
20/30 INDEFLATOR -REF 1000184 WPL2122268-01 (2019-03-01)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Vascular
4 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 20, 2022
Back to Nature Cheddalicious Cheese Flavored Crackers 6 oz.. UPC: 8-19898-01491-0 6 cartons per case
High riskUsing this product could cause serious injury, illness or death — stop using it now.B&G Foods North America, Inc.
FDA (openFDA food enforcement)
Reported Apr 20, 2022
LIPOSORBER System, Model: LA-15, consisting of: Apheresis machine, product# 101445 model: MA-03, and disposables…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kaneka America Corp.
FDA (openFDA device enforcement)
Reported Apr 20, 2022
Access-9 Large Bore Hemostasis Valves, Catalog Code: 580775001, IN8112/C, K05-00053H, K05-00109G, K05-00137K,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merit Medical Systems, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 20, 2022
Cub 2 Enclosed Bed Canopy System
High riskUsing this product could cause serious injury, illness or death — stop using it now.Sensory Medical Inc.
FDA (openFDA device enforcement)
Reported Apr 20, 2022
SKIPPY Reduced Fat Creamy Peanut Butter NET WT 40 oz (2 LB 8 OZ) 1.13 kg UPC 037600105200 packaged in clear plastic jar…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Skippy Foods, LLC.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Apr 13, 2022
Alinity m HBV Application Specification File (US and CE)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Molecular, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 13, 2022
Brius Pontics (components in a set of custom metal orthodontic devices);BRIUS , RX Only, Non-Sterile, Custom Made…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Brius Technologies Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 13, 2022
DeRoyal ST Neonatal Dressing Change Kit, containing Prevantics antiseptic (chlorhexidine gluconate and isopropyl…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DeRoyal Industries Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 13, 2022
Panther Fusion GBS Assay Cartridges 96 Tests, Catalog Number: PRD-04484. in vitro diagnostic test for group b…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hologic, Inc.
FDA (openFDA device enforcement)
Reported Apr 13, 2022
Cardiohelp-i Transport Guard with Transport Guard (701072525): is a blood oxygenation and carbon dioxide removal system…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Maquet Medical Systems USA
FDA (openFDA device enforcement)
Reported Apr 13, 2022
MODEL: X-RAY R/F SYSTEM FLUOROspeed X1
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Shimadzu Medical Systems
2 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 13, 2022
BenchMark ULTRA and DISCOVERY ULTRA Instruments
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ventana Medical Systems Inc.
FDA (openFDA device enforcement)
Reported Apr 13, 2022
SyncVision Systems, Model: 400-0100.10, PN: 30000485688x, with software version 4.2.x
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Volcano Corporation
FDA (openFDA device enforcement)
Reported Apr 6, 2022
Liko Universal Twinbar 670 QRH, an accessory that can be used together with most Liko lifts, model numbers 3156087 and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 6, 2022
Les Fermes Cavendish Farms Frozen Original Hash Brown Potato Patties Net Wt, 42.3 (1.2 kg). 12 retail packages per…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Cavendish Farms
FDA (openFDA food enforcement)
Reported Apr 6, 2022
FORE-SIGHT ELITE Absolute Tissue Oximeter, REF: 01-06-3000, Contents: Monitor 1 EA., Accessory Kit 1 EA.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Edwards Lifesciences, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 6, 2022
Biolox delta Ceramic V40 Femoral Head 32/ -4.0mm Catalog Number: 6570-0-032
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Howmedica Osteonics Corp.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 6, 2022
Illumina NextSeq 550Dx, REF: 20005715, CE, IVD
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Illumina, Inc.
FDA (openFDA device enforcement)
Reported Apr 6, 2022
MiniMed 630G: MMT-1715, MMT-1754, MMT-1755; MiniMed 670G: MMT-1740, MMT-1741, MMT-1742, MMT-1760, MMT-1761, MMT-1762,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic MiniMed
FDA (openFDA device enforcement)
Reported Apr 6, 2022
Revogene, For In Vitro Diagnostic use in performing nucleic acid testing in clinical laboratories. Meridian branded…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Meridian Bioscience Inc.
FDA (openFDA device enforcement)
Reported Apr 6, 2022
Mevion S250 and S250i Proton Therapy Systems hand pendant (P/N 10263 or P/N 37808)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mevion Medical Systems, Inc.
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.