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. 1,909 recalls have been distributed to Utah in the last 12 months.

49,677 total recalls
1,909 in last 12 months

Showing 2052120540 of 49,677 recalls

Medical DeviceOctober 7, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: Software versions syngo CT VB20 running on the following Siemens Recalled by...

The Issue: Software issue identified in the software versions syngo CT VB20 running on...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2019· Beckman Coulter, Inc.

Recalled Item: UniCel DxH Slidemaker Stainer (DxH SMS) and UniCel DxH Slidemaker Recalled...

The Issue: When the UniCel DxH Slidemaker Stainer and UniCel DxH Slidemaker Stainer II...

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

Class II — Potential Health HazardOngoing
DrugOctober 7, 2019· Mylan Laboratories Limited (Sterile Products Division)

Recalled Item: Rifampin for Injection Recalled by Mylan Laboratories Limited (Sterile...

The Issue: Failed Impurities/Degradation Specifications: discoloration due to elevated...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
FoodOctober 7, 2019· Dole Packaged Foods, LLC

Recalled Item: Dole Crushed Pineapple in 100% pineapple juice Manufactured For Dole...

The Issue: Foreign object; potential plastic pieces.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 7, 2019· Nova Ortho-Med Inc

Recalled Item: Star 8 Rolling Walker/Rollator Recalled by Nova Ortho-Med Inc Due to Walkers...

The Issue: Walkers within the identified serial range have the potential for the front...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2019· Baxter Healthcare Corporation

Recalled Item: Prismaflex Control Unit Recalled by Baxter Healthcare Corporation Due to...

The Issue: Communication error alarms may result in interruption of therapy, delay in...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2019· Baxter Healthcare Corporation

Recalled Item: Prismaflex Control Unit Recalled by Baxter Healthcare Corporation Due to...

The Issue: Communication error alarms may result in interruption of therapy, delay in...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2019· Neocis Inc.

Recalled Item: Neocis Guidance System Fiducial Array - Product Usage: The Neocis Recalled...

The Issue: The Fiducial Array may mismatch their measurement files resulting in failed...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2019· Baxter Healthcare Corporation

Recalled Item: Prismaflex Control Unit Recalled by Baxter Healthcare Corporation Due to...

The Issue: Communication error alarms may result in interruption of therapy, delay in...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2019· Teleflex Medical

Recalled Item: WECK AutoEndo5 Recalled by Teleflex Medical Due to Certain clip appliers...

The Issue: Certain clip appliers have an increase in misloading and/or jamming related...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2019· Teleflex Medical

Recalled Item: WECK Hem-O-Lok AutoEndo5 Recalled by Teleflex Medical Due to Certain clip...

The Issue: Certain clip appliers have an increase in misloading and/or jamming related...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2019· ICU Medical, Inc.

Recalled Item: Recalled by ICU Medical, Inc. Due to There is a potential that IV...

The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2019· ICU Medical, Inc.

Recalled Item: Recalled by ICU Medical, Inc. Due to There is a potential that IV...

The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2019· ICU Medical, Inc.

Recalled Item: Recalled by ICU Medical, Inc. Due to There is a potential that IV...

The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2019· ICU Medical, Inc.

Recalled Item: Recalled by ICU Medical, Inc. Due to There is a potential that IV...

The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2019· ICU Medical, Inc.

Recalled Item: 111" 10 Drop Admin Set w/2 Inj Sites Recalled by ICU Medical, Inc. Due to...

The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2019· ICU Medical, Inc.

Recalled Item: Recalled by ICU Medical, Inc. Due to There is a potential that IV...

The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2019· ICU Medical, Inc.

Recalled Item: Recalled by ICU Medical, Inc. Due to There is a potential that IV...

The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2019· ICU Medical, Inc.

Recalled Item: Recalled by ICU Medical, Inc. Due to There is a potential that IV...

The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2019· ICU Medical, Inc.

Recalled Item: Recalled by ICU Medical, Inc. Due to There is a potential that IV...

The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...

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

Class II — Potential Health HazardOngoing