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 8941–8960 of 30,153 recalls

Medical DeviceDecember 23, 2021· GE Healthcare, LLC

Recalled Item: GE Healthcare MR superconducting magnets Recalled by GE Healthcare, LLC Due...

The Issue: The magnetic resonance systems could potentially have a cryogen ventilation...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2021· GE Healthcare, LLC

Recalled Item: GE Healthcare MR superconducting magnets Recalled by GE Healthcare, LLC Due...

The Issue: The magnetic resonance systems could potentially have a cryogen ventilation...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2021· GE Healthcare, LLC

Recalled Item: GE Healthcare MR superconducting magnets Recalled by GE Healthcare, LLC Due...

The Issue: The magnetic resonance systems could potentially have a cryogen ventilation...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2021· GE Healthcare, LLC

Recalled Item: GE Healthcare MR superconducting magnets Recalled by GE Healthcare, LLC Due...

The Issue: The magnetic resonance systems could potentially have a cryogen ventilation...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2021· GE Healthcare, LLC

Recalled Item: GE Healthcare MR superconducting magnets Recalled by GE Healthcare, LLC Due...

The Issue: The magnetic resonance systems could potentially have a cryogen ventilation...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2021· GE Healthcare, LLC

Recalled Item: GE Healthcare MR superconducting magnets Recalled by GE Healthcare, LLC Due...

The Issue: The magnetic resonance systems could potentially have a cryogen ventilation...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2021· GE Healthcare, LLC

Recalled Item: GE Healthcare MR superconducting magnets Recalled by GE Healthcare, LLC Due...

The Issue: The magnetic resonance systems could potentially have a cryogen ventilation...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2021· GE Healthcare, LLC

Recalled Item: GE Healthcare MR superconducting magnets Recalled by GE Healthcare, LLC Due...

The Issue: The magnetic resonance systems could potentially have a cryogen ventilation...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2021· GE Healthcare, LLC

Recalled Item: GE Healthcare MR superconducting magnets Recalled by GE Healthcare, LLC Due...

The Issue: The magnetic resonance systems could potentially have a cryogen ventilation...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2021· GE Healthcare, LLC

Recalled Item: GE Healthcare MR superconducting magnets Recalled by GE Healthcare, LLC Due...

The Issue: The magnetic resonance systems could potentially have a cryogen ventilation...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2021· GE Healthcare, LLC

Recalled Item: GE Healthcare MR superconducting magnets Recalled by GE Healthcare, LLC Due...

The Issue: The magnetic resonance systems could potentially have a cryogen ventilation...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2021· Olympus Corporation of the Americas

Recalled Item: Spiration Valve System (SVS) Valve in Cartridge -A one-way endobronchial...

The Issue: Mislabeled Patient Charge Label indicating model number SVS-V7-00 (7mm)...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2021· Synthes (USA) Products LLC

Recalled Item: Universal Chuck-The Universal Chuck is an Instrument Handle provided as...

The Issue: Top cap may loosen and detach if the Universal Chuck becomes jammed and the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2021· Boston Scientific Corporation

Recalled Item: JAGTOME RX 39-30-260-025 Material Number: M00573100 Recalled by Boston...

The Issue: Sterility of device is compromised due to a sterile barrier breach

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2021· Boston Scientific Corporation

Recalled Item: HYDRATOME RX 44-30MM/450CM Material Number: M00583070 Recalled by Boston...

The Issue: Sterility of device is compromised due to a sterile barrier breach

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2021· Boston Scientific Corporation

Recalled Item: JAGTOME RX 39-20-260-025 Material Number: M00573080 Recalled by Boston...

The Issue: Sterility of device is compromised due to a sterile barrier breach

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2021· Boston Scientific Corporation

Recalled Item: JAGTOME REVOLUTION RX 39-20-450-025 Material Number: M00584250 Recalled by...

The Issue: Sterility of device is compromised due to a sterile barrier breach

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2021· Boston Scientific Corporation

Recalled Item: DREAMTOME 49-20MM/450CM Material Number: M00584020 Recalled by Boston...

The Issue: Sterility of device is compromised due to a sterile barrier breach

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2021· Boston Scientific Corporation

Recalled Item: Dreamtome RX Cannulating Sphincterotome-DREAMTOME 44-20MM/260CM Material...

The Issue: Sterility of device is compromised due to a sterile barrier breach

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2021· Boston Scientific Corporation

Recalled Item: JAGTOME RX 49-30-450-035 Material Number: M00573030 Recalled by Boston...

The Issue: Sterility of device is compromised due to a sterile barrier breach

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

Class II — Potential Health HazardOngoing