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 48,100 notices were distributed nationwide, so they reach New Jersey too — those are in the archive.
Reported Sep 27, 2023
Philips Tempus Pro Patient Monitor, REF: 00-1004-R, 00-1007-R, 00-1024-R, 00-1026-R, 00-1004, and 00-1007, when Used…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Remote Diagnostic Technologies Ltd.
FDA (openFDA device enforcement)
Reported Sep 20, 2023
Proclaim XR 5 Implantable Pulse Genterator REF 3660 (previously known as Proclaim" 5 Elite IPG) Model 3660 Product…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Abbott Medical
6 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 20, 2023
FILMARRAY Gastrointestinal (GI) Panel (Part No.: RFIT-ASY-0104 & RFIT-ASY-0116) Pouch Module Software
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioFire Diagnostics, LLC
FDA (openFDA device enforcement)
Reported Sep 20, 2023
ACUSON Redwood 2.0 ultrasound systems, REF: 11503314
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Sep 13, 2023
ZVU Functional GI Software, REF: ZVU-3
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Diversatek Healthcare
FDA (openFDA device enforcement)
Reported Sep 13, 2023
ISee Ortho-K Lens
Moderate riskThis product could cause temporary or reversible health problems — stop using it.PARAGON VISION SCIENCES, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 13, 2023
M/L Taper Hip Prosthesis Extended Offset, Reduced Neck Length, Size 4 (Item Number 00771100640) and Size 6 (Item Number…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, Inc.
FDA (openFDA device enforcement)
Reported Sep 6, 2023
Upper roller bracket (part number 1088370) for the Gen2 gantry enclosure for the Radixact Treatment Delivery System.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Accuray Incorporated
FDA (openFDA device enforcement)
Reported Sep 6, 2023
LIF AMP, Adjustable Awl, REF 117-165, Part of the AMP System. Used with Spine Lateral Interbody Systems, IdentiTi LIF,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alphatec Spine, Inc.
FDA (openFDA device enforcement)
Reported Sep 6, 2023
Beckman Coulter, IVD, REF: OSR61171, IgA, 4 x 14 mL R1, 4 x 11 mL R2
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
FDA (openFDA device enforcement)
Reported Sep 6, 2023
The following items sold at Stop & Shop stores located in the New York Metro Region: Natures Promise Lemonade Natures…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C & S Wholesale Grocers Inc.
7 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 30, 2023
BioFire Respiratory Panel 2.1 (RP2.1), REF: 423742, For FILMARRAY systems, IVD, Rx Only
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioFire Diagnostics, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 30, 2023
Green Curry Paste (one ounce) 28g contained in Every Plate meal code 87, 116.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Every Plate
FDA (openFDA food enforcement)
Reported Aug 30, 2023
Soft Serve on the Go brand Vanilla Chocolate flavor; 8 fl oz; UPC 0-91404-15129-0 Soft Serve on the Go brand Parve…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Real Kosher Ice Cream, Inc.
4 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 30, 2023
ADVIA Chemistry Urinary/Cerebrospinal Fluid Protein (UCFP), Material Number 11319151, in vitro diagnostic use in the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Aug 25, 2023
FSIS Issues Public Health Alert for Shoprite Brand Bowl & Basket Chicken Noodle Soup Due to Misbranding and Undeclared…
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Kettle Cuisine Midco, LLC
USDA FSIS
Reported Aug 23, 2023
Benton's 100 Calorie Snack Packs Baked Chocolate Wafer Snacks 6-0.81 OZ (23g) Packs Net Wt. 4.86 oz UPC: 4 099100…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Commercial Bakeries
7 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 23, 2023
Alpenfest Style Sachertote NET WT 17.6 OZ (1 LB 1.6OZ) 500g Frozen UPC:2010 0889 Packaged in Cardboard Carton.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lidl US TRADING
FDA (openFDA food enforcement)
Reported Aug 23, 2023
Medtronic REF 46915 Duet External Drainage and Monitoring system, Interlink Injection sites, Ventricular Catheter,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Neurosurgery
FDA (openFDA device enforcement)
Reported Aug 23, 2023
Newly Weds Foods R03810 LOEFFLER COMP PORK ROLL CURE X1 54lbs
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Newly Weds Foods, Inc.
3 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 16, 2023
Randox RX Series Urea Enzymatic Kinetic Assay Ref. Numbers: (1) UR3825 (2) UR3873 (3) UR8334 (4) UR8070 (Modena)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Randox Laboratories Ltd.
FDA (openFDA device enforcement)
Reported Aug 9, 2023
Impella RP Flex with SmartAssist intracardiac microaxial blood pump, Product Number 1000323
High riskUsing this product could cause serious injury, illness or death — stop using it now.Abiomed, Inc.
FDA (openFDA device enforcement)
Reported Aug 9, 2023
Outshine No Sugar Added Strawberry Fruit Bars Brand name: Outshine; Unit size:14.7 fl oz carton with 6 bars; Container…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dreyer's Grand Ice Cream, Inc.
FDA (openFDA food enforcement)
Reported Aug 9, 2023
E.N.A. Meat Packing Inc. Recalls Frozen, Raw Beef and Lamb Products Produced Without Benefit of Inspection
High riskUsing this product could cause serious injury, illness or death — stop using it now.E.N.A. Meat Packing Inc.
USDA FSIS
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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.