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 2102121040 of 30,153 recalls

Medical DeviceJune 16, 2016· Ab Sciex

Recalled Item: AB SCIEX QTRAP¿ 4500MD LC/MS/MS System Mass Spectrometer for In-Vitro...

The Issue: MultiQuant MD software where under certain conditions a user can be...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2016· Ab Sciex

Recalled Item: AB Sciex API 3200MD" LC/MS/MS System. In-Vitro Diagnostic Instrument Part...

The Issue: MultiQuant MD software where under certain conditions a user can be...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2016· Medtronic Inc., Cardiac Rhythm and Heart Failure

Recalled Item: Medtronic Recalled by Medtronic Inc., Cardiac Rhythm and Heart Failure Due...

The Issue: This Pacing Lead System does not comply with Section 8.5.2.3 of IEC 60601-1,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2016· Ab Sciex

Recalled Item: AB SCIEX Triple Quad 4500MD LC/MS/MS System. Mass Spectrometer for Recalled...

The Issue: MultiQuant MD software where under certain conditions a user can be...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2016· Ab Sciex

Recalled Item: AB SCIEX 3200MD QTRAP¿ LC/MS/MS System Mass Spectrometer for In-Vitro...

The Issue: MultiQuant MD software where under certain conditions a user can be...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2016· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: A7 Anesthesia Delivery System Recalled by Mindray DS USA, Inc. dba Mindray...

The Issue: Potential for a leak to occur on the back-up O2 and air e-size cylinder...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2016· Smith & Nephew, Inc.

Recalled Item: Smith and Nephew TWINFIX QUICK-T Knot Pusher Suture Cutter Recalled by Smith...

The Issue: The device could be subject to breaches of its sterile packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2016· WalkMed Infusion, LLC

Recalled Item: T095-120 IV Set with 1.2 Micron Filter. Packaged in a Tyvek pouch Recalled...

The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2016· Hill-Rom, Inc.

Recalled Item: Volker 2080 Recalled by Hill-Rom, Inc. Due to The current construction of...

The Issue: The current construction of the side rail latch may not be able to support...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2016· WalkMed Infusion, LLC

Recalled Item: T095-022 Recalled by WalkMed Infusion, LLC Due to WalkMed Infusion, LLC...

The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2016· WalkMed Infusion, LLC

Recalled Item: T090-022V 90" 20 Drop IV Admin Set Needle free Y-Site Recalled by WalkMed...

The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2016· WalkMed Infusion, LLC

Recalled Item: T100-000F Recalled by WalkMed Infusion, LLC Due to WalkMed Infusion, LLC...

The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2016· WalkMed Infusion, LLC

Recalled Item: T100-022WF Recalled by WalkMed Infusion, LLC Due to WalkMed Infusion, LLC...

The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2016· WalkMed Infusion, LLC

Recalled Item: Spike Set Recalled by WalkMed Infusion, LLC Due to WalkMed Infusion, LLC...

The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2016· WalkMed Infusion, LLC

Recalled Item: T030-000 -30" 20 Drop IV Admin Secondary Set. Packaged in a Tyvek pouch...

The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2016· WalkMed Infusion, LLC

Recalled Item: T100-000VF Recalled by WalkMed Infusion, LLC Due to WalkMed Infusion, LLC...

The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2016· WalkMed Infusion, LLC

Recalled Item: T090-000W 90" 20 Drop IV Admin Set w/2 Needlefree Y-Sites Recalled by...

The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2016· WalkMed Infusion, LLC

Recalled Item: T105-000WC IV Set w/2 Y-Sites Recalled by WalkMed Infusion, LLC Due to...

The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2016· WalkMed Infusion, LLC

Recalled Item: T100-120F with 1.2 micron filter and FP Clip. Packaged in a Tyvek pouch...

The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2016· WalkMed Infusion, LLC

Recalled Item: The pump (with cushioning foam inserts) is packaged in a Recalled by WalkMed...

The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of the Triton...

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

Class II — Potential Health HazardOngoing