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. 2,666 recalls have been distributed to Utah in the last 12 months.

49,677 total recalls
2,666 in last 12 months

Showing 30613080 of 28,579 recalls

Medical DeviceSeptember 4, 2024· LEICA BIOSYSTEMS NUSSLOCH GMBH

Recalled Item: Leica Biosystems Cryostat Model Number CM1510 S Recalled by LEICA BIOSYSTEMS...

The Issue: As part of our post market surveillance, we recognized that some customers...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2024· LEICA BIOSYSTEMS NUSSLOCH GMBH

Recalled Item: Leica Biosystems Cryostat Model Number CM1950 Recalled by LEICA BIOSYSTEMS...

The Issue: As part of our post market surveillance, we recognized that some customers...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2024· Howmedica Osteonics Corp.

Recalled Item: Triathlon Universal TS Baseplate Size 2 - A single use Recalled by Howmedica...

The Issue: Anterior locking tabs on the Triathlon Universal Baseplate are out of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: (1) Centurion Sterile CirClamp Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Product has been identified as having holes in the packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2024· Philips North America Llc

Recalled Item: SmartPath to dStream for XR and 3.0T- For use as Recalled by Philips North...

The Issue: Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2024· Philips North America Llc

Recalled Item: Ingenia 3.0T - For use as a diagnostic device to obtain cross-sectional...

The Issue: Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2024· Philips North America Llc

Recalled Item: Ingenia Ambition S - For use as a diagnostic device Recalled by Philips...

The Issue: Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2024· Philips North America Llc

Recalled Item: Ingenia 3.0T CX - For use as a diagnostic device Recalled by Philips North...

The Issue: Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2024· Philips North America Llc

Recalled Item: Evolution Upgrade 3.0T - For use as a diagnostic device Recalled by Philips...

The Issue: Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2024· Philips North America Llc

Recalled Item: Ingenia Elition X- For use as a diagnostic device to Recalled by Philips...

The Issue: Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2024· Philips North America Llc

Recalled Item: SmartPath to dStream for 1.5T - For use as a Recalled by Philips North...

The Issue: Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2024· Philips North America Llc

Recalled Item: Ingenia Ambition X - For use as a diagnostic device Recalled by Philips...

The Issue: Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2024· Philips North America Llc

Recalled Item: Ingenia 1.5T -For use as a diagnostic device to obtain cross-sectional...

The Issue: Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2024· Philips North America Llc

Recalled Item: SmartPath to Ingenia Elition X - For use as a Recalled by Philips North...

The Issue: Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2024· Philips North America Llc

Recalled Item: Ingenia Elition S -For use as a diagnostic device to Recalled by Philips...

The Issue: Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2024· Philips North America Llc

Recalled Item: MR 5300 - For use as a diagnostic device to obtain cross-sectional images...

The Issue: Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2024· Philips North America Llc

Recalled Item: MR 7700 -For use as a diagnostic device to obtain cross-sectional images...

The Issue: Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2024· Blue Ortho

Recalled Item: Predict+ is a data-driven Recalled by Blue Ortho Due to Predict+ is being...

The Issue: Predict+ is being recalled for lack of pre-market clearance/approval.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2024· Merit Medical Systems, Inc.

Recalled Item: Melrose Wakefield Hospital Injector And Syringe Recalled by Merit Medical...

The Issue: Due to a manufacturing process resulting in holes/breaches in the Tyvek...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2024· Merit Medical Systems, Inc.

Recalled Item: Monarch Inflation Device 30 atm/bar MAP152 AssessPLUS Large Bore Hemostasis...

The Issue: Due to a manufacturing process resulting in holes/breaches in the Tyvek...

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

Class II — Potential Health HazardOngoing