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 Apr 27, 2016
OraQuick HCV Visual Reference Panel Intended to assist new operation in becoming proficient at reading specimens with…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.OraSure Technologies, Inc.
FDA (openFDA device enforcement)
Reported Apr 27, 2016
Peru Food Mote Corn Maiz Mote Net Wt. 15 oz. Imported and distributed by: Peru Food Import Inc.PO Box 419 West New…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Peru Food Import Inc.
FDA (openFDA food enforcement)
Reported Apr 27, 2016
Extended Brilliance Workspace NM Nuclear medicine image display and processing application suite. AutoSPECT Pro…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 27, 2016
Siemens SOMATOM Definition: Intended to produce cross-sectional images of the body. Computed tomography (CT) x-ray…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 27, 2016
Cervical Spine Locking Plate (CSLP) System, 4mm Cancellous Self Tapping Screw, Length 16mm Lot # 9666776 and 4mm Cortex…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes (USA) Products LLC
FDA (openFDA device enforcement)
Reported Apr 20, 2016
The Concerto Basic Shower Trolley is intended for assisted hygiene care, especially showering and bathing of residents…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arjo, Inc. dba ArjoHuntleigh
FDA (openFDA device enforcement)
Reported Apr 20, 2016
Arthrex Deltoid Ligament Reconstruction Implant System. Intended as a fixation post, a distribution bridge or for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arthrex, Inc.
FDA (openFDA device enforcement)
Reported Apr 20, 2016
BD-Retic-Count Reticulocyte Reagent System; Hematology: Used for in vitro diagnostics
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Becton, Dickinson and Company, BD Biosciences
FDA (openFDA device enforcement)
Reported Apr 20, 2016
Bumble Bee Chunk Light Tuna in Water, 48cans/case, 5oz, UPC 8660000020
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bumble Bee Foods LLC
2 more products in this recall
FDA (openFDA food enforcement)
Reported Apr 20, 2016
Cygnus Medical First StepBedside ADDWATER Kit,non-sterile. First Step in cleaning flexible endoscopes. SKU# EP-6W (The…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Cygnus Medical
FDA (openFDA device enforcement)
Reported Apr 20, 2016
GE Healthcare, Aisys CS2 anesthesia..
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Medical Systems, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 20, 2016
Diana Automated Compounding System, Diana Onco Plus, Item No. ASN220 The Diana is an automated compounding device for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 20, 2016
MATLAW'S Raw - EZ Peel - Deveined - Shell On Shrimp. NET WT. 2 LBS (32 OZ.) .907 KG (8-12 COUNT PER POUND), packaged in…
High riskUsing this product could cause serious injury, illness or death — stop using it now.National Fish & Seafood, Inc.
FDA (openFDA food enforcement)
Reported Apr 20, 2016
Neurotherm NT2000iX RF Generator Model Number: RFG-NT -2000iX
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Neurotherm, Inc.
FDA (openFDA device enforcement)
Reported Apr 20, 2016
Brilliance 64:Computed Tomography X-ray Systems, Intended to produce cross-sectional images of the body by computer…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 20, 2016
RTI Surgical Streamline Occipito-Cervico-Thoracic (OCT) Final Driver, Common Name: Screw Driver
Moderate riskThis product could cause temporary or reversible health problems — stop using it.RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)
FDA (openFDA device enforcement)
Reported Apr 20, 2016
Burger King Liquid Frying Oil, Net Wt. 35 LB (15.9 kg), Miami, Florida 33126, UPC 2 06 75258 06956 3
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stratas Foods LLC
4 more products in this recall
FDA (openFDA food enforcement)
Reported Apr 20, 2016
Spetzler Claw Tip, Universal - 5450-800-311 Spetzler Open Angle Micro Claw Tip, Universal - 5450-800-313 The Spetzler…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Instruments Div.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 20, 2016
SYNTHECEL Dura Repair, 510K # K131792, K113071, Class II, Classification name: Dura Substitute Device listing number:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes (USA) Products LLC
5 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 20, 2016
USE (Ebony) PTA .014" rapid exchange (RX) Peripheral Dilatation Catheter. Distributed by US Endovascular, St. Louis, MO.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.US Endovascular
FDA (openFDA device enforcement)
Reported Apr 20, 2016
Blue Ridge Farms Vinegar & Oil Cole Slaw, 03010, Net Weight: 1 X 10 LB., Keep Refrigerated; Use by: 3/09/16, 3/20/16,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Winter Gardens Quality Foods, Inc.
9 more products in this recall
FDA (openFDA food enforcement)
Reported Apr 13, 2016
Cittero Mortadella, packaged in deli bags. This is a deli service item.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Bj Wholesale Club
70 more products in this recall
FDA (openFDA food enforcement)
Reported Apr 13, 2016
Simplexa HSV 1&2 Direct (MOL2150) with Direct Amplification Disc (MOL1451, MOL1452, MOL1455) Model Number: MOL2150,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Focus Diagnostics Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 13, 2016
Fresenius Hemoflow F3 Dialyzer Part Number: 0520165A Indicated for Acute and Chronic Hemodialysis
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fresenius Medical Care Renal Therapies Group, LLC
1 more product 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.