Product Recalls in Utah

Product recalls affecting Utah — including food, drugs, consumer products, medical devices, and vehicles distributed to Utah. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,075 recalls have been distributed to Utah in the last 12 months.

49,677 total recalls
1,075 in last 12 months

Showing 13721–13740 of 49,677 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· 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 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· Hill-Rom, Inc.

Recalled Item: Liko Mobile Lifts: Primarily intended for use in nursing homes Liko M220...

The Issue: Missing bushing on Liko M220 and M230 causing wear and potential for patient...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2021· Intuitive Surgical, Inc.

Recalled Item: da Vinci Xi and X 12-8 mm Conductive Cannula Reducer Recalled by Intuitive...

The Issue: Conductive Cannula Reducer metal tip may get dislodged from the plastic...

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 Cannulating Sphincterotome-DREAMTOME 44-20MM/450CM 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: HYDRATOME RX 49-30MM/260CM Material Number: M00583010 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: RX CHOLANGIOGRAM KIT - SINGLE Material Number: M00575240 M00575240 M00575280...

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 44-30-260-035 Material Number: M00573060 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 39-30-450-025 Material Number: M00573110 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 44-30-450-035 Material Number: M00573070 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 44-20-450-035 Material Number: M00573050 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 39-30-260-025 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· Empowered Diagnostics LLC

Recalled Item: CovClear COVID-19 Rapid Antigen Test Recalled by Empowered Diagnostics LLC...

The Issue: COVID test kits were offered for sale and distributed to consumers in the...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 22, 2021· Philips Respironics, Inc.

Recalled Item: Trilogy Evo Recalled by Philips Respironics, Inc. Due to Philips has...

The Issue: Philips has identified a specific lot of non-conforming material...

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

Class I — Serious Health HazardOngoing