Recalls distributed in New York
These notices name New York 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.
6,374 stored notices name New York, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,132 notices were distributed nationwide, so they reach New York too — those are in the archive.
Reported Jun 15, 2016
Ellipse ND: YAG Laser applicator for Ellipse Multiflex Medical Laser Products.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ellipse A/S
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 15, 2016
GE Revolution CT The system is intended for head, whole body, cardiac and vascular X-ray Computed Tomography…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 15, 2016
4 ml FX Sodium Fluoride/Potassium Oxalate tube, Ref 454297 VACUETTE Glycolytic Inhibitor Tubes contain an…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Greiner Bio-One North America, Inc.
FDA (openFDA device enforcement)
Reported Jun 15, 2016
Nuvi Global StemVitae Multivitamin 30oz.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Nuvi Global Corporation
FDA (openFDA food enforcement)
Reported Jun 15, 2016
Potassium CHLORide added to 5% Dextrose Injection, 20 mEq 250 mL Bag, PharMEDium Services, LLC, 6100 Global Drive,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pharmedium Services, LLC
FDA (openFDA drug enforcement)
Reported Jun 15, 2016
Philips Healthcare DigitalDiagnost stationary X-ray system
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Healthcare
8 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 15, 2016
Sedecal SA Mobile Diagnost w DR x-ray system
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sedecal USA, Inc.
FDA (openFDA device enforcement)
Reported Jun 15, 2016
Sterile Sheridan/HVT Cuffed, Murphy Eye, Tracheal Tube, Ref: V5-10314, ID: 7.0 mm, Rx Only, Manufactured by: Teleflex…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical
FDA (openFDA device enforcement)
Reported Jun 15, 2016
Werner Brand Butter Toffee Peanuts, net wt. 2.25 oz, UPC 7 09972 80113 3 Werner Brand Butter Toffee Peanuts, net wt. 6…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Werner Gourmet Meat Snacks, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jun 15, 2016
Persona Trabecular Metal Tibia; Persona Trabecular Metal Tibial Plate Instruments and Modular Brackets; Used to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
FDA (openFDA device enforcement)
Reported Jun 14, 2016
G & M Co. Recalls Beef Products Due To Possible E. Coli O157:H7 Contamination
High riskUsing this product could cause serious injury, illness or death — stop using it now.G&M Co.
USDA FSIS
Reported Jun 13, 2016
Asian Jade Customs Brokerage Recalls Sausage Products Distributed Without Benefit of Import Inspection
High riskUsing this product could cause serious injury, illness or death — stop using it now.Asian Jade Customs Brokerage
USDA FSIS
Reported Jun 8, 2016
The ARCHITECT Estradiol Kit Intended to measure estradiol, an estrogenic steroid, in plasma.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Laboratories
FDA (openFDA device enforcement)
Reported Jun 8, 2016
CytoScan¿ Dx Assay. The CytoScan Dx Assay consists of five reagent modules, wash buffers (WS), a microarray kit, and…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Affymetrix Inc.
FDA (openFDA device enforcement)
Reported Jun 8, 2016
Non-Vented Dispensing Pin with One-Way Valve and Luer Lock Ultrasite Valve Product Usage: Used for aspiration of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.B. Braun Medical, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 8, 2016
Hip Preservation System Signature Series PreBent Burs under the following labels: 1) PreBent Spherical Bur, 5.5mm x…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ConMed Corporation
FDA (openFDA device enforcement)
Reported Jun 8, 2016
Monaco RTP System Product Usage: The Monaco system is used to make treatment plans for patients with prescriptions for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Jun 8, 2016
Novation Ceramic AHS Cluster-Hole Shell, Plasma Coated, 54mm, O.D. (Acetabular Cup), Catalog Number 140-01-54; For use…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Exactech, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 8, 2016
Integra MicroFrance Monopolar and Bipolar Electrosurgical Instruments
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corp.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 8, 2016
Angel Wings Complete Daily Multi with 146 nutrients including Anti-aging and Superfruit Antioxidants and 75 Plant…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Liquid Assets Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jun 8, 2016
AllergiEnd ST-9 Multiple Skin Test Applicator (Item 1000) and AllergiEnd ST-9 Multiple Well Test Tray (Item (1001).…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medscience Inc.
FDA (openFDA device enforcement)
Reported Jun 8, 2016
Replacement HEPA filter for Natus Sterile-Drier Model 43 and Model 44. Filter Catalogue Part Number: 54343, 54344, and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Natus Medical Incorporated
FDA (openFDA device enforcement)
Reported Jun 8, 2016
Fresh Long Chili Peppers, Raw, 10 lb box. Imported from Dominican Republic.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Patel Shippers Inc.
FDA (openFDA food enforcement)
Reported Jun 8, 2016
Brilliance 64 Computed Tomography X-ray Systems Product Usage: Intended to produce cross-sectional images of the body…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
3 more products in this recall
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.