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.

6,478 stored notices name New York, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,853 notices were distributed nationwide, so they reach New York too — those are in the archive.

Medical devices

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)

Food

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)

Medical devices

Reported Jan 11, 2017

Boston Scientific, INGEVITY" MRI Leads, Sterile EO, RxOnly.

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

Boston Scientific Corporation

FDA (openFDA device enforcement)

Food

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)

Food

Reported Jan 11, 2017

Ashby's Sterling Peanut Butter Landslide Ice Cream, 3 gallon container, frozen

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

House Of Flavors, Inc.

FDA (openFDA food enforcement)

Medical devices

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)

Food

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)

Food

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)

Meat & poultry

Reported Jan 9, 2017Updated Oct 23, 2026

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)

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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.