All recall categories

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 48,122 notices were distributed nationwide, so they reach New York too — those are in the archive.

Meat & poultry

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

Medical devices

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)

Food

Reported Jan 4, 2017

Kerry Upgrade Bio WS, Net Wt. 50 lb (22068 kg), Item 5R01451.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Kerry, Inc.

FDA (openFDA food enforcement)

Drugs

Reported Jan 4, 2017

CVS Health Homeopathic Infants Teething Tablets 135 count bottle Distributed by: CVS Pharmacy, Inc. One CVS Drive,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Raritan Pharmaceuticals, Inc.

2 more products in this recall

FDA (openFDA drug enforcement)

Medical devices

Reported Jan 4, 2017

Shimadzu X-ray TV System, Catalog No. SONIALVISION G4

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Shimadzu Medical Systems

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 4, 2017

SOMATOM Scope, Computed tomography x-ray system

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Siemens Medical Solutions USA, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jan 4, 2017

DRIED SILVER FISH, N.W. 30 LBS, PRODUCT OF CHINA

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Wd Import and Export Inc.

FDA (openFDA food enforcement)

Medical devices

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)

Medical devices

Reported Dec 28, 2016

ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 5 F Stiffened Micro-Introducer Kit, 45CM SS/SS…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Angiodynamics, Inc.

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

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)

Drugs

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)

Medical devices

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)

Food

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)

Food

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)

Medical devices

Reported Dec 28, 2016

Affinity Fusion" Oxygenator with Integrated Arterial Filter, Affinity Fusion cardiotomy/Venous Reservoir, Perfusion…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medtronic Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

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)

Food

Reported Dec 28, 2016

Heihujiaoyupai, USA jiazhoufengwei, Fish, NET WT 4.2oz (120g)

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Midwest International Corp.

3 more products in this recall

FDA (openFDA food enforcement)

Medical devices

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)

Medical devices

Reported Dec 28, 2016

OrthoPediatrics PediNail Intramedullary Nailing System 4.5mm X 48mm Cortical Screw

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

OrthoPediatrics Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 28, 2016

DELFIA hFSH kit. In Vitro Diagnostic for the determination of hFSH in serum

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

PerkinElmer Health Sciences, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 28, 2016

PerkinElmer 20ul Clear RoboRack Tip, Pipette (Qty 960) Item Number: 6000677. Used with the: JANUS AUTOMATED WORKSTATION…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

PerkinElmer, Inc.

FDA (openFDA device enforcement)

Food

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)

Medical devices

Reported Dec 28, 2016

Ingenia MR-OR; 781437, 781438 The MR-OR option is intended for allowing transfer of a neurosurgical patient from OR…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Philips Electronics North America Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Dec 28, 2016

AQURE System Software Version 2.2.0 Model #: 933-599 UDI: (01)05700699335999(10)2.2.0 Catalog number: 933-599 The AQURE…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Radiometer America 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.