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. 2,639 recalls have been distributed to Utah in the last 12 months.

49,677 total recalls
2,639 in last 12 months

Showing 58415860 of 28,579 recalls

Medical DeviceJuly 13, 2023· EMPATICA SRL

Recalled Item: Embrace2- Indicated for use as an adjunct to seizure monitoring Recalled by...

The Issue: May have a battery life lasting less than the full 48 hours, requiring the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2023· Instrumentation Laboratory

Recalled Item: ACL TOP Family 50 Series Models as follows: In vitro Recalled by...

The Issue: Sample misidentification could occur under specific conditions and patient...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2023· Siemens Medical Solutions USA, Inc.

Recalled Item: ACUSON Redwood 2.0 ultrasound systems Recalled by Siemens Medical Solutions...

The Issue: If a user-generated preset for an 18L6 transducer created on a 1.0...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2023· Beckman Coulter Inc.

Recalled Item: Beckman Coulter Recalled by Beckman Coulter Inc. Due to Lipemic interference...

The Issue: Lipemic interference failed to meet the performance specification listed...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2023· Olympus Corporation of the Americas

Recalled Item: The Air/Water Valve is provided/used with the following Endoscopes:...

The Issue: The air/water valve MAJ-1444 used with OER-Pro and OER-Elite may become...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2023· Medicrea International

Recalled Item: IMPIX S Recalled by Medicrea International Due to There is a potential for a...

The Issue: There is a potential for a product packaging non-conformity issue which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2023· Medicrea International

Recalled Item: IMPIX C+ Recalled by Medicrea International Due to There is a potential for...

The Issue: There is a potential for a product packaging non-conformity issue which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2023· Medicrea International

Recalled Item: IMPIX MANTA Recalled by Medicrea International Due to There is a potential...

The Issue: There is a potential for a product packaging non-conformity issue which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2023· Draeger Medical, Inc.

Recalled Item: Carina Sub-Acute Care Ventilator Recalled by Draeger Medical, Inc. Due to...

The Issue: Presence of polyether polyurethane (PE-PUR) and emission of...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 12, 2023· Medicrea International

Recalled Item: IMPIX ALIF Recalled by Medicrea International Due to There is a potential...

The Issue: There is a potential for a product packaging non-conformity issue which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2023· Medicrea International

Recalled Item: GRANVIA-C Recalled by Medicrea International Due to There is a potential for...

The Issue: There is a potential for a product packaging non-conformity issue which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2023· Medicrea International

Recalled Item: IMPIX MANTA+ Recalled by Medicrea International Due to There is a potential...

The Issue: There is a potential for a product packaging non-conformity issue which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2023· Medicrea International

Recalled Item: IMPIX DLIF Recalled by Medicrea International Due to There is a potential...

The Issue: There is a potential for a product packaging non-conformity issue which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2023· Medicrea International

Recalled Item: IMPIX 3D Recalled by Medicrea International Due to There is a potential for...

The Issue: There is a potential for a product packaging non-conformity issue which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2023· Medicrea International

Recalled Item: IMPIX TLIF Recalled by Medicrea International Due to There is a potential...

The Issue: There is a potential for a product packaging non-conformity issue which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2023· Medicrea International

Recalled Item: PASS LP Recalled by Medicrea International Due to There is a potential for a...

The Issue: There is a potential for a product packaging non-conformity issue which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2023· Medicrea International

Recalled Item: IMPIX ALIF S/A Recalled by Medicrea International Due to There is a...

The Issue: There is a potential for a product packaging non-conformity issue which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2023· Abbott Diabetes Care, Inc.

Recalled Item: FreeStyle Libre 2 Readers Recalled by Abbott Diabetes Care, Inc. Due to If...

The Issue: If blood glucose monitoring system users attempt to start a new sensor, when...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2023· Medtronic Sofamor Danek USA, Inc

Recalled Item: CD HORIZON Spinal System Solera Awl Tip Tap Recalled by Medtronic Sofamor...

The Issue: Incorrect Laser Marking - Solera Awl Tip Tap

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH Gamma-Glutamyl Transferase-IIn vitro diagnostic use in the...

The Issue: Potential for reagent carryover on the Atellica CH 930 resulting in a...

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

Class II — Potential Health HazardOngoing