Product Recalls in New York

Product recalls affecting New York — including food, drugs, consumer products, medical devices, and vehicles distributed to New York. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,703 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,703 in last 12 months

Showing 1940119420 of 55,896 recalls

Medical DeviceSeptember 24, 2020· Zimmer Biomet, Inc.

Recalled Item: ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene Recalled by...

The Issue: Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugSeptember 23, 2020· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: RIOMET ER (metformin hydrochloride for extended-release oral suspension)...

The Issue: CGMP Deviations: Detection of N-nitrosodimethylamine (NDMA) impurity in...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 23, 2020· Hale And Hearty Soups, LLC

Recalled Item: WILD MUSHROOM BARLEY soup Recalled by Hale And Hearty Soups, LLC Due to...

The Issue: Product may contain pieces of maggots.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 22, 2020· Gordian Surgical

Recalled Item: TroClose 1200 - Product Usage: intended for use in a variety of gynecologic...

The Issue: Endotoxin test results found above the acceptable levels in LAL test (above...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2020· Cardinal Health 200, LLC

Recalled Item: Kangaroo Connect 1000ml Bag Set Recalled by Cardinal Health 200, LLC Due to...

The Issue: The feeding spike sets may leak at the interface of the tube and spike...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2020· Pentax of America Inc

Recalled Item: 9310HD Digital Video Capture Module with software version 3.4.0 or Recalled...

The Issue: There is an intermittent software issue that could affect the systems, in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2020· Boston Scientific Corporation

Recalled Item: Visual-ICE MRI Cryoablation System Mobile Connection Panel (Visual-ICE MRI...

The Issue: Incorrectly installed base.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2020· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Chemistry Systems-Fructosamine (FRUC)-For in vitro diagnostic use in...

The Issue: Fructosamine QC and patient samples may exhibit a 60 umol/L positive bias...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2020· Pentax of America Inc

Recalled Item: 9372HD Digital Capture (ver. 1.1.0 + w/ 9263 endoPortal) Recalled by Pentax...

The Issue: There is an intermittent software issue that could affect the systems, in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2020· Cardinal Health 200, LLC

Recalled Item: Kangaroo Connect 500ml Bag Set Recalled by Cardinal Health 200, LLC Due to...

The Issue: The feeding spike sets may leak at the interface of the tube and spike...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2020· Flexicare Medical Ltd.

Recalled Item: ProVu Single Use Video Stylet with ET Tube Recalled by Flexicare Medical...

The Issue: When the video stylet cuff is over-inflated there is potential for occlusion...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 22, 2020· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH Systems Fructosamine (FRUC)-For in vitro diagnostic use in...

The Issue: Fructosamine QC and patient samples may exhibit a 60 umol/L positive bias...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2020· GE Healthcare, LLC

Recalled Item: Revolution Apex Recalled by GE Healthcare, LLC Due to There is a potential...

The Issue: There is a potential for a smudge artifact that could be suspect for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2020· Stryker Neurovascular

Recalled Item: Trevo XP ProVue Retriever Recalled by Stryker Neurovascular Due to Increase...

The Issue: Increase in fracture complaints of the flexible, tapered core wire,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 21, 2020· Stereotaxis Inc

Recalled Item: Niobe ES System Recalled by Stereotaxis Inc Due to There is a potential for...

The Issue: There is a potential for fire in the inside computer cabinet.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Artis one systems with a Display Port transceiver-Fluoroscopic X-Ray...

The Issue: Potential malfunction in which the examination room monitor may become...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2020· Smith & Nephew, Inc.

Recalled Item: Genesis (GII) - Product Usage: designed for use in patients Recalled by...

The Issue: The anterior locking detail does not meet its design specifications.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2020· Smith & Nephew, Inc.

Recalled Item: 5.5MM Arthrogarde Hip Access Cannula Recalled by Smith & Nephew, Inc. Due to...

The Issue: The J Lock feature on the cannula body was manufactured incorrectly,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodSeptember 21, 2020· Wismettac Asian Foods, INC

Recalled Item: Shirakiku brand Black Fungus (Kikurage) Recalled by Wismettac Asian Foods,...

The Issue: California Department of Public Health sampled and tested Shirakiku brand...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 19, 2020· Dianne's Fine Desserts

Recalled Item: Devonshire Bake Shop brand Lemon Italian Cream Cake Recalled by Dianne's...

The Issue: Product contains undeclared peanuts.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund