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.
4,816 stored notices name New Jersey, reported between Jun 20, 2012 and Nov 11, 2026. A further 48,765 notices were distributed nationwide, so they reach New Jersey too — those are in the archive.
Reported Sep 25, 2024
ERIC Retrieval Device REF: ER173020 ER174030 ER176044 The ERIC Retrieval Device is a mechanical thrombectomy device…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Microvention Inc.
FDA (openFDA device enforcement)
Reported Sep 25, 2024
Bliss Tree Ragi Butter Murukku 200g UPC:8906087451754. Packaged in a box, 13 boxes per case Bliss Tree Ragi Butter…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sri Lakshmi Narasimhar Overseas
5 more products in this recall
FDA (openFDA food enforcement)
Reported Sep 18, 2024
American Outdoor Products - Astronaut Strawberries, packaged in 0.5oz (14g) metallic plastic pouches. Sold individually…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.American Outdoor Products, Inc.
FDA (openFDA food enforcement)
Reported Sep 18, 2024
FILMARRAY 2.0 INSTRUMENT, REF: FLM2-ASY-0001, FLM2-ASY-0001-W
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 Sep 18, 2024
IBA Proton Therapy System - PROTEUS 235 ProteusPLUS and ProteusONE Software versions: PTS-8 versions, PTS-10 versions,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ion Beam Applications S.A.
FDA (openFDA device enforcement)
Reported Sep 18, 2024
Atellica CH Urinary/Cerebrospinal Fluid Protein (UCFP); Siemens Material Number (SMN): 11097543
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
7 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 18, 2024
Brand Name: Vit-l-escence Product Name: Vit-l-escence Singles A3 Model/Catalog Number: 1203- Software Version: N/A…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ultradent Products, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 11, 2024
BD Pyxis QFill Replenishment Station, REF: 138904-01, medication cabinet system
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 11, 2024
LVP Primary Administration Set, Dual-Inlet, Low-Sorbing, Needle-Free Port, Y-Site (Qty 25), Product Code: SET-0013-25.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Fresenius Kabi USA, LLC
FDA (openFDA device enforcement)
Reported Sep 11, 2024
Sevoflurane E_Vap.(Quik-Fil):used with the A9 Anesthesia System-Used to provide the vapor of an anesthetic agent with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mindray DS USA, Inc. dba Mindray North America
3 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 11, 2024
a.) Great Value 8oz Apple Juice in 6pack; PET plastic bottle b.) Great Value 96oz Apple Juice; PET plastic bottle c.)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Refresco Beverages US Inc.
FDA (openFDA food enforcement)
Reported Sep 11, 2024
Heparin, Gore Viabahn VBX, Balloon Expandable Endoprosthesis, for the following Reference numbers: United States:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.W L Gore & Associates, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 4, 2024
FreeStyle Libre 3 Sensors, REF: 72081-01, component of the FreeStyle Libre 3 Continuous Glucose Monitoring System
High riskUsing this product could cause serious injury, illness or death — stop using it now.Abbott Diabetes Care, Inc.
FDA (openFDA device enforcement)
Reported Sep 4, 2024
DR 800. Digital Radiography X-ray System.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Agfa N.V.
FDA (openFDA device enforcement)
Reported Sep 4, 2024
DxI 9000 Access Immunoassay Analyzer, Catalog #C11137.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter, Inc.
FDA (openFDA device enforcement)
Reported Sep 4, 2024
Yummy brand Swirly Ices Tropical Tornado flavor Net Wt. 2.3 ounces (65g)x 8 popsicles, Total Net Wt. 18.34 ounces…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Paradise Distributors, LLC
4 more products in this recall
FDA (openFDA food enforcement)
Reported Sep 4, 2024
CVS Health brand and HEB Baby brand Premium Infant Formula with Iron Milk-Based Powder; packaged in 964g composite…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.PBM Nutritionals, LLC
FDA (openFDA food enforcement)
Reported Sep 4, 2024
Prime Food brand Steam Bun with Egg Custard Added; 10pcs/pack; NET WT. 20 oz (1lb.4 oz) 568g; KEEP FROZEN; INGREDIENTS:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Prime Food Processing Corp.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Aug 28, 2024
Shahzada brand Pulses and Spices; Cinnamon Powder; 7 oz (200g); packaged in clear plastic zip-top bags
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Advance Food International Inc.
FDA (openFDA food enforcement)
Reported Aug 28, 2024
Healthy Living Acetaminophen, Aspirin (NSAID) and Caffeine, tablets USP, 250 mg/250 mg/65 mg, 100-count bottles,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Aurobindo Pharma USA Inc.
FDA (openFDA drug enforcement)
Reported Aug 28, 2024
McGrath Mac Video Laryngoscope, REF: 300-000-000 , Non-Sterile, Rx Only
High riskUsing this product could cause serious injury, illness or death — stop using it now.Covidien
2 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 28, 2024
ClotTriever XL Catheter, 30 mm, REF: 41-102, used with Instructions for Use ClotTriever XL Catheter ClotTriever…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Inari Medical - Oak Canyon
FDA (openFDA device enforcement)
Reported Aug 28, 2024
IBA Proton Therapy System - PROTEUS 235- Designed to produce and deliver a proton beam for the treatment of patients…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ion Beam Applications S.A.
FDA (openFDA device enforcement)
Reported Aug 28, 2024
GM60A. Digital Diagnostic Mobile X-Ray System.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.NeuroLogica Corporation
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.