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. 2,776 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,776 in last 12 months

Showing 1534115360 of 30,153 recalls

Medical DeviceDecember 21, 2018· Philips Medical Systems Nederlands

Recalled Item: Panorama 1.0T Recalled by Philips Medical Systems Nederlands Due to There is...

The Issue: There is a potential for the ceiling speaker(s) to fall from their position...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2018· Philips Medical Systems Nederlands

Recalled Item: Intera 0.5T Standard Recalled by Philips Medical Systems Nederlands Due to...

The Issue: There is a potential for the ceiling speaker(s) to fall from their position...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2018· Philips Medical Systems Nederlands

Recalled Item: Achieva 1.5T Recalled by Philips Medical Systems Nederlands Due to There is...

The Issue: There is a potential for the ceiling speaker(s) to fall from their position...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2018· Philips Medical Systems Nederlands

Recalled Item: Intera 1.5T High Performance Recalled by Philips Medical Systems Nederlands...

The Issue: There is a potential for the ceiling speaker(s) to fall from their position...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2018· Cook Inc.

Recalled Item: Check-Flo Performer Introducer Recalled by Cook Inc. Due to The products...

The Issue: The products were manufactured with longer than specified sheaths.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2018· Steris Corporation

Recalled Item: AMSCO 5000 Series Washer/Disinfector Model # 5052 Recalled by Steris...

The Issue: The software in the systems may not process the cycle originally intended....

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2018· Steris Corporation

Recalled Item: AMSCO 3000 Series Washer/Disinfector Model # 3052 Recalled by Steris...

The Issue: The software in the systems may not process the cycle originally intended....

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2018· Merge Healthcare, Inc.

Recalled Item: The WinStation Retinal Imager Recalled by Merge Healthcare, Inc. Due to...

The Issue: Certain configurations of Merge Eye Station hardware may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2018· GE Healthcare, LLC

Recalled Item: GE Healthcare Centricity Universal Viewer Breast Imaging Centricity...

The Issue: When switching back & forth between multiple UV instances in the Windows...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2018· TERRIFIC CARE LLC

Recalled Item: CoaguChek XS PT Test Recalled by TERRIFIC CARE LLC Due to Potential for...

The Issue: Potential for abnormally high INR test results with the CoaguChek XS PT Test...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 19, 2018· Associates of Cape Cod, Inc.

Recalled Item: Fungitell Kit Recalled by Associates of Cape Cod, Inc. Due to The kits may...

The Issue: The kits may contain the incorrect number of components or the kits may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2018· Reckitt Benckiser LLC

Recalled Item: Durex Pleasure Pack (60 ct) Recalled by Reckitt Benckiser LLC Due to Five...

The Issue: Five batches of the product have failed the specification of 1.0kPa for...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2018· Reckitt Benckiser LLC

Recalled Item: Durex Real Feel Recalled by Reckitt Benckiser LLC Due to Five batches of the...

The Issue: Five batches of the product have failed the specification of 1.0kPa for...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2018· Cook Inc.

Recalled Item: Entuit Secure Gastrointestinal Suture Anchor Set Recalled by Cook Inc. Due...

The Issue: There is a potential for difficulty in sliding down the retention mechanism...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2018· Cook Inc.

Recalled Item: Entuit Secure Gastrointestinal Suture Anchor Set Recalled by Cook Inc. Due...

The Issue: There is a potential for difficulty in sliding down the retention mechanism...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2018· Boston Scientific Corporation

Recalled Item: Stingray" Guidewire Recalled by Boston Scientific Corporation Due to A batch...

The Issue: A batch of 185cm Stingray Guidewires are incorrectly labeled as 300cm...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2018· Cincinnati Sub-Zero Products LLC, a Gentherm Company

Recalled Item: Hemotherm CE Dual Reservoir Cooler/Heater Recalled by Cincinnati Sub-Zero...

The Issue: Evidence supports that when customers performed a fuse replacement as part...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2018· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity TF PET/CT (non-RoHS) Recalled by Philips Medical Systems...

The Issue: A software update is being issued to correct multiple issues identified in...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2018· Cochlear Americas Inc.

Recalled Item: Cochlear Baha 5 Sound Processor Tamper Proof Battery Door (3 pcs.) Recalled...

The Issue: Product was packaged with the Incorrect tamper proof battery door.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2018· Insulet Corporation

Recalled Item: Omnipod DASH Insulin Management System Recalled by Insulet Corporation Due...

The Issue: There is a potential for a communication interruption following a bolus...

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

Class II — Potential Health HazardOngoing