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 Jan 18, 2017
Reprocessed Ablation Catheter Cable Catalog Number: CR3425CT, CR3434CT Ablation catheter cables are designed as…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Sustainability Solutions
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 18, 2017
Non Fat Dry Milk, Grade A - High Heat in 50 # bags , manufactured by Valley Milk Products. Stasburg, Virginia 22657 ,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Valley Milk Products
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jan 18, 2017
Eclipse Treatment Planning System version 13.MR2 [13.06.31 with Smart Segmentation Knowledge Based Contouring version…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Varian Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Jan 12, 2017
Kettle Cuisine, LLC Recalls Chicken Soup Product Due to Misbranding and Undeclared Allergens
High riskUsing this product could cause serious injury, illness or death — stop using it now.Kettle Cuisine Midco, LLC
USDA FSIS
Reported Jan 11, 2017
MULLIGATAWNY, Net wt 6.9 lbs, UPC 1 80644 00041 0, packaged in a heat sealed flexible plastic bag.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hale And Hearty Soups, LLC
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jan 11, 2017
G3 Opticage Expandable Interbody Fusion Device, Model No. 9180-00, 9180-01, 9180-06, 9180-07, 9180-17, 9101-00, 9101-06…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Interventional Spine Inc.
FDA (openFDA device enforcement)
Reported Jan 11, 2017
Refrigerated, Ready to Eat Herring in Brine with no brand name, packaged in bulk 25 lb. white plastic bucket and…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Royal Seafood Baza, Inc.
16 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 11, 2017
Tipiak Pearled Couscous Easy cooking 12.3 Oz (350g) Item Number: 10020450803 Product of France
Moderate riskThis product could cause temporary or reversible health problems — stop using it.TIPIAK Inc.
FDA (openFDA food enforcement)
Reported Jan 9, 2017
Schreiber Processing Corp. Recalls Chicken Tender Products Due to Possible Foreign Matter Contamination and Misbranding
High riskUsing this product could cause serious injury, illness or death — stop using it now.Schreiber Processing Corporation
USDA FSIS
Reported Jan 4, 2017
Innova 2000
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
12 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 4, 2017
Specimen Gate Laboratory 5002-0180, Specimen Gate eReports 5002-0370, Software Version 1.0 Specimen Gate Laboratory is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.PerkinElmer Health Sciences, Inc.
FDA (openFDA device enforcement)
Reported Dec 28, 2016
CyberKnife Robotic Radiosurgery Systems, models: G3, G4, VSI. Radiology: The CyberKnife Robotic Radiosurgery System is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Accuray Incorporated
FDA (openFDA device enforcement)
Reported Dec 28, 2016
Gammex Non-Latex Sensitive Neoprene Surgical Gloves Ansell Lanka (pvt) Ltd. Biyagama Export Processing Zone, Biyagama,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ansell Healthcare Products LLC
FDA (openFDA device enforcement)
Reported Dec 28, 2016
BD SurePathTM Preservative Collection Vials, catalog numbers 490505, 490527, 491095, 491096, and 491097. SurePath¿…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
FDA (openFDA device enforcement)
Reported Dec 28, 2016
C-PAV/PHENTOL/PGE1, All strengths, All sizes, Rx only, Colonia Care Pharmacy, Colonia NJ 07067
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Colonia Care Pharmacy
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Dec 28, 2016
Equinoxe Reverse Shoulder Fixed Angle Torque Defining Screw Kit
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Exactech, Inc.
FDA (openFDA device enforcement)
Reported Dec 28, 2016
FAIRWAY LIKE NO OTHER MARKET brand CANDY CORN, of varying weight, Item Code 228402 XXXXXX -- The product is packaged in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fairway Group Holding Corp. dba Fairway Bakery LLC
FDA (openFDA food enforcement)
Reported Dec 28, 2016
Rx CHOICE brand LIQUID VITAMIN C, 16 FL OZ (473 mL), NDC 50383-167-16 --- HI-TECH PHARMACAL CO., INC. Amityville, NY…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Hi-Tech Pharmacal Co., Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Dec 28, 2016
Merge OrthoCase software. The firm name on the label is Merge Healthcare, Hartland, WI.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merge Healthcare, Inc.
FDA (openFDA device enforcement)
Reported Dec 28, 2016
Algovita Spinal Cord Stimulation System, Percutaneous Leads, 8-Electrode Percutaneous Lead Kit; Algovita Spinal Cord…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nuvectra
FDA (openFDA device enforcement)
Reported Dec 28, 2016
OSCOR ADELANTE BREEZEWAY 8F C55¿ S61CM D66CM Catalog # AB081040 Is designed to facilitate the introduction of catheters…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Oscor, Inc.
29 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 28, 2016
Phil-Am Smoked Mackerel (Hasa Hasa) Net. Wt. 200g (7.05 oz.) packaged: Clear flexible plastic pouch and is topped by a…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Phil-Am Trading, Inc.
FDA (openFDA food enforcement)
Reported Dec 28, 2016
8450-107-530 3.0MM Precision Match Head, 13CM, single use, Sterile The Stryker MIS (Minimally Invasive Surgery) product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Instruments Div.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 28, 2016
Sermorelin/GHRP-6 Injection 6 mg-3 mg Lyophylized I, 2 mL vial, Rx, Town and Country Compounding and Consultation…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Town and Country Compounding and Consultation Services
FDA (openFDA drug 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.