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.
4,822 stored notices name New Jersey, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,784 notices were distributed nationwide, so they reach New Jersey too — those are in the archive.
Reported Dec 28, 2022
Centricity PACS-IW with Universal Viewer version 5.0. Used to display medical images (Including mammograms) and data…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Medical Systems, LLC
14 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 28, 2022
The Natus Cranial Access Kit is designed to be a complete, single use and disposable accessory and instrumentation set…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Natus Medical Incorporated
FDA (openFDA device enforcement)
Reported Dec 28, 2022
X-CORE 2 Ti Core, Static. Part of the NuVasive X-Core Expandable VBR System used with spinal fixation.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.NuVasive Inc.
FDA (openFDA device enforcement)
Reported Dec 28, 2022
Utopia brand Enoki Mushroom; Utopia Foods Inc; 200g; Product of China; Distributed by Utopia Foods Inc.; UPC…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Utopia Foods Inc.
FDA (openFDA food enforcement)
Reported Dec 21, 2022
DeRoyal MINOR ORAL / ENT PACK, REF 89-2576.15
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DeRoyal Industries Inc.
155 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 14, 2022
Small Joint OATS Set, REF AR-8981-06S, 6mm; and Small Joint OATS Set, REF AR-8981-08S, 8mm, both containing a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arthrex, Inc.
FDA (openFDA device enforcement)
Reported Dec 14, 2022
0.9% Sodium Chloride Injection USP 1000 mL Single-dose container Rx only NDC 0264-5802-00 B. Braun Medical Inc.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.B. Braun Medical, Inc.
FDA (openFDA drug enforcement)
Reported Dec 14, 2022
ARASHAN brand mixed dried fruit packaged in 1lb clear plastic bags with a sticker label. UPC: 850008491368
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bek12 Inc.
FDA (openFDA food enforcement)
Reported Dec 14, 2022
Boston Baking Mini Crumb Cake - individually wrapped - 3 oz. Storage Instructions: 10 months frozen, 7 days ambient…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Boston Baking Inc.
FDA (openFDA food enforcement)
Reported Dec 14, 2022
2.5 mm LifePort Endotracheal Tube Adapters 10-pack, Catalog: 9025; and 2.5 mm LifePort Endotracheal Tube Adaptors…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bunnell, Inc.
FDA (openFDA device enforcement)
Reported Dec 14, 2022
LineSider Spinal System 5.5/6.0mm, Non-mod Standard 7.1mm - Dual Lead, Non-cannulated. Thoracolumbosacral pedicle screw…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integrity Implants Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 14, 2022
Propel Mini Mometasone Furoate Sinus Implant, with Straight Delivery System, REF 60044
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intersect ENT, Inc.
FDA (openFDA device enforcement)
Reported Dec 14, 2022
Nestle Toll House Edible Chocolate Chip Cookie Dough packaged in 15oz tubs - 4 tubs per case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nestle-USA, Inc. (Corporate Office)
FDA (openFDA food enforcement)
Reported Dec 14, 2022
IgA Immunoturbidimetric Assay- In vitro determination of IgA and IgM in serum and plasma Catalog Number: IA3832
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Randox Laboratories Ltd.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 14, 2022
Weis Quality Premium Ice Cream Sea Salt Caramel Ripple 1.5 Quart (1.42 L) UPC 041497-01288
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Weis Markets, Inc., Ice Cream Division
FDA (openFDA food enforcement)
Reported Dec 7, 2022
Accelerate PhenoTest BC kit REF 10101018
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Accelerate Diagnostics Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 7, 2022
Alcon Custom Pak Surgical Procedure Pack
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alcon Research, LLC
FDA (openFDA device enforcement)
Reported Dec 7, 2022
CMV IgM EIA, in vitro diagnostic.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bio-Rad Laboratories, Inc.
FDA (openFDA device enforcement)
Reported Dec 7, 2022
CoViPoint COVID test kit (MultiPLEX/Direct) Kit Item Numbers: BC-DK0200; BM-AD4K0200 BM-ADK0200 BM-CDK0200 BM-CFDK0200…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GS Biomark LLC
FDA (openFDA device enforcement)
Reported Nov 30, 2022
Tiramisu Twist Cookie 3.4 oz. packaged in a gold bag with a large image of two cookies on the package. SKU…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Daiso California Warehouse
FDA (openFDA food enforcement)
Reported Nov 23, 2022
Pedialyte Unflavored Electrolyte Solution 2 fl oz plastic reclosable bottle 12-4 packs in a case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Laboratories
11 more products in this recall
FDA (openFDA food enforcement)
Reported Nov 23, 2022
Superion¿ Indirect Decompression System (IDS) Model Numbers and Size: 101-9808 - 8mm 01-9812 - 12mm 101-9814 - 14mm
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Neuromodulation Corporation
FDA (openFDA device enforcement)
Reported Nov 23, 2022
Extension Tabletop for Operating Table System 1140, Model Nos. 1140.20F0 and 1140.20AN
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Getinge USA Sales Inc.
FDA (openFDA device enforcement)
Reported Nov 23, 2022
Visualase Cooled Laser Applicator System (VCLAS) 9735560 .4MM CORE FIBER 10MM TIP product. Used to necrotize or…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Navigation, Inc.
FDA (openFDA device enforcement)
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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.