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. 2,495 recalls have been distributed to Utah in the last 12 months.

49,677 total recalls
2,495 in last 12 months

Showing 2026120280 of 28,579 recalls

Medical DeviceApril 22, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: BIOGRAPH mCT Flow 20-4R Recalled by Siemens Medical Solutions USA Inc. Due...

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware of a potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: BIOGRAPH mCT Flow 40-3R Recalled by Siemens Medical Solutions USA Inc. Due...

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware of a potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: BIOGRAPH Sys 40-3R to 40-4R Recalled by Siemens Medical Solutions USA Inc....

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware of a potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: SYS IVK Recalled by Siemens Medical Solutions USA Inc. Due to Siemens...

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware of a potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: BIOGRAPH mCT Flow 64-3R Recalled by Siemens Medical Solutions USA Inc. Due...

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware of a potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: BIOGRAPH mCT Flow Edge-3R Recalled by Siemens Medical Solutions USA Inc. Due...

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware of a potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: BIOGRAPH mCT Flow 40-4R Recalled by Siemens Medical Solutions USA Inc. Due...

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware of a potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: BIOGRAPH 64 - 3 Ring Recalled by Siemens Medical Solutions USA Inc. Due to...

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware of a potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: Biograph mCT-S(64) 3R Recalled by Siemens Medical Solutions USA Inc. Due to...

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware of a potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: BIOGRAPH mCT S(20)-4R Recalled by Siemens Medical Solutions USA Inc. Due to...

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware of a potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2016· Baxter Healthcare Corp.

Recalled Item: GEM(TM) Recalled by Baxter Healthcare Corp. Due to Instructions for use...

The Issue: Instructions for use booklet may puncture the outer Tyvek lid.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2016· Draeger Medical, Inc.

Recalled Item: Draeger D-Vapor/ D-Vapor 3000 Vaporizers with Baxter Desflurane Agent and...

The Issue: Operators noticed unwanted release of evaporating anesthetic agent at the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2016· Miami Fat Supply, Inc

Recalled Item: The Red Head 2 Reusable Fat Harvesting Canister Recalled by Miami Fat...

The Issue: During an FDA inspection it was found that the products are marketed without...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2016· Baxter Healthcare Corp.

Recalled Item: GEM(TM) Recalled by Baxter Healthcare Corp. Due to Instructions for use...

The Issue: Instructions for use booklet may puncture the outer Tyvek lid.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2016· Baxter Healthcare Corp.

Recalled Item: GEM(TM) Recalled by Baxter Healthcare Corp. Due to Instructions for use...

The Issue: Instructions for use booklet may puncture the outer Tyvek lid.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2016· Musculoskeletal Transplant Foundation, Inc.

Recalled Item: Musculoskeletal Transplant Foundation Recalled by Musculoskeletal Transplant...

The Issue: AFT Diverted Tubes are being recalled due to a customer complaint involving...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2016· Baxter Healthcare Corp.

Recalled Item: GEM(TM) Recalled by Baxter Healthcare Corp. Due to Instructions for use...

The Issue: Instructions for use booklet may puncture the outer Tyvek lid.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2016· Baxter Healthcare Corp.

Recalled Item: GEM(TM) Recalled by Baxter Healthcare Corp. Due to Instructions for use...

The Issue: Instructions for use booklet may puncture the outer Tyvek lid.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2016· Acorn Stairlifts, Inc

Recalled Item: Acorn 130 Stairlift Recalled by Acorn Stairlifts, Inc Due to The design of...

The Issue: The design of the seats did not consistently have the adequate strength...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2016· Ortho-Clinical Diagnostics

Recalled Item: The VITROS¿ Chemistry Products Calibrator Kit 31 Recalled by Ortho-Clinical...

The Issue: There is an incorrect value (data/calibration mathematics) on ADDs. This...

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

Class III — Low RiskOngoing