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. 1,173 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
1,173 in last 12 months

Showing 10521–10540 of 30,153 recalls

Medical DeviceFebruary 26, 2021· Stryker Corporation

Recalled Item: Stryker Recalled by Stryker Corporation Due to Their is a potential that...

The Issue: Their is a potential that Video Processor/Illuminators may exhibit...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: Interventional Fluoroscopic X-Ray System - Product Usage: developed for...

The Issue: Siemens has become aware of a potential issue in which the imaging system...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2021· Heartware, Inc.

Recalled Item: Instructions for Use and Patient Manual for HeartWare HVAD System. Recalled...

The Issue: IFU and Patient Manual updated to describe HVAD Controller Connection...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2021· Heartware, Inc.

Recalled Item: Instructions for Use and Patient Manual for HeartWare HVAD System. Recalled...

The Issue: Medtronic HeartWare HVAD System Instructions for Use (IFU) and Patient...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 25, 2021· Cardinal Health 200, LLC

Recalled Item: In-View Clear Leggings Sterile Recalled by Cardinal Health 200, LLC Due to...

The Issue: Cardinal Health has determined that a manufacturing variance in a plastic...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2021· Fenwal Inc

Recalled Item: Amicus Exchange Kit - Product Usage: intended for use in Recalled by Fenwal...

The Issue: Some lots of Amicus MNC Apheresis and Amicus Exchange kits have leaking...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2021· Fenwal Inc

Recalled Item: Amicus MNC Apheresis Kit - Double Needle - Product Usage: Recalled by Fenwal...

The Issue: Some lots of Amicus MNC Apheresis and Amicus Exchange kits have leaking...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2021· Tenacore LLC

Recalled Item: Alaris Infusion Pump 8100 Bezel (plastic piece only) Recalled by Tenacore...

The Issue: Bezel repair parts used, not by the original manufacturer, to service and...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 25, 2021· Fenwal Inc

Recalled Item: Amicus Exchange Kit Therapeutics - Product Usage: intended for use Recalled...

The Issue: Some lots of Amicus MNC Apheresis and Amicus Exchange kits have leaking...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2021· Tenacore LLC

Recalled Item: Alaris Infusion Pump Module Recalled by Tenacore LLC Due to Bezel repair...

The Issue: Bezel repair parts used, not by the original manufacturer, to service and...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 25, 2021· Cardinal Health 200, LLC

Recalled Item: In-View Clear Leggings Sterile Non-Sterile Recalled by Cardinal Health 200,...

The Issue: Cardinal Health has determined that a manufacturing variance in a plastic...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2021· Cardinal Health 200, LLC

Recalled Item: Femoral Angiography Drape Bulk Non-Sterile Recalled by Cardinal Health 200,...

The Issue: Cardinal Health has determined that a manufacturing variance in a plastic...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2021· Cardinal Health 200, LLC

Recalled Item: Femoral Angiography Drape Sterile Recalled by Cardinal Health 200, LLC Due...

The Issue: Cardinal Health has determined that a manufacturing variance in a plastic...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2021· Cardinal Health 200, LLC

Recalled Item: In-View Clear Leggings Bulk Non-Sterile Recalled by Cardinal Health 200, LLC...

The Issue: Cardinal Health has determined that a manufacturing variance in a plastic...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2021· Philips Healthcare (Suzhou) Co., Ltd.

Recalled Item: Philips CT systems are advanced continuous-rotation computed tomography...

The Issue: Philips has internally detected an issue with the actuators used in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2021· Arthrex, Inc.

Recalled Item: Drill Bit Recalled by Arthrex, Inc. Due to The color indicator on the...

The Issue: The color indicator on the proximal end of the shaft of the AR-8770-02 is...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2021· Trinity Sterile, Inc.

Recalled Item: Midline Catheter Dressing Change Kit with Statlock - Product Usage: Recalled...

The Issue: Evidence of face masks or other material in the seal in several kits,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2021· DePuy Orthopaedics, Inc.

Recalled Item: The ATTUNE¿ Rotating Platform (RP) Total Knee System - Product Recalled by...

The Issue: Globally the company is removing 37 lots affected lots for MBT & ATTUNE (S+)...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2021· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: Mindray BeneVision Distributed Monitoring System( DMS) 1. p/n 115-051209-00...

The Issue: BeneVision DMS may intermittently freeze and require a manual reboot after...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2021· DePuy Orthopaedics, Inc.

Recalled Item: ATTUNE¿ FIXED BEARING KNEE - Product Usage: composed of individually...

The Issue: Globally the company is removing 37 lots affected lots for MBT & ATTUNE (S+)...

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

Class II — Potential Health HazardOngoing