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. 2,621 recalls have been distributed to Utah in the last 12 months.

49,677 total recalls
2,621 in last 12 months

Showing 1072110740 of 28,579 recalls

Medical DeviceNovember 12, 2020· Hill-Rom Manufacturing, Inc.

Recalled Item: Life2000 Ventilation System Recalled by Hill-Rom Manufacturing, Inc. Due to...

The Issue: Under certain conditions, there is a risk for fire.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2020· Canon Medical System, USA, INC.

Recalled Item: Canon PET-CT SCANNER Recalled by Canon Medical System, USA, INC. Due to A...

The Issue: A software problem has been identified which could result in the diagnostic...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2020· Westmed, Inc.

Recalled Item: Recalled by Westmed, Inc. Due to There is a potential that the fitment...

The Issue: There is a potential that the fitment between the oxygen delivery tube and...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2020· Westmed, Inc.

Recalled Item: (Adult Elongated O2/CO2 Mask - Product Usage: intended Recalled by Westmed,...

The Issue: There is a potential that the fitment between the oxygen delivery tube and...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2020· Westmed, Inc.

Recalled Item: Adult Elongated CO2/O2 Mask Recalled by Westmed, Inc. Due to There is a...

The Issue: There is a potential that the fitment between the oxygen delivery tube and...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2020· Westmed, Inc.

Recalled Item: Recalled by Westmed, Inc. Due to There is a potential that the fitment...

The Issue: There is a potential that the fitment between the oxygen delivery tube and...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2020· Westmed, Inc.

Recalled Item: Recalled by Westmed, Inc. Due to There is a potential that the fitment...

The Issue: There is a potential that the fitment between the oxygen delivery tube and...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2020· Westmed, Inc.

Recalled Item: Westmed DISPOSABLE RESPIRATORY PRODUCTS NON-REBREATHER MASK Recalled by...

The Issue: There is a potential that the fitment between the oxygen delivery tube and...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2020· Terumo Cardiovascular Systems Corporation

Recalled Item: (1) Capiox FX25 (West) Advance Oxygenator- with left port Recalled by Terumo...

The Issue: Capiox FX25 Advance oxygenator may be the incorrect configuration (East vs....

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2020· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation 4 Recalled by RAYSEARCH LABORATORIES AB Due to Two issues were...

The Issue: Two issues were found with the treatment plan report: 1) There may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2020· Integra LifeSciences Corp.

Recalled Item: Instruction Manual for Mayfield A2000 Skull Cap - Product Usage: Recalled by...

The Issue: Revised Instruction Manual to the most accurate illustration for Mayfield...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2020· WELCH ALLYN, INC/MORTARA

Recalled Item: ELI 380 Electrocardiograph - Product Usage: intended to be a...

The Issue: The radio within the device can become disassociated with the wireless...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2020· Baxter Healthcare Corporation

Recalled Item: MiniCap Extended Life PD Transfer Set Recalled by Baxter Healthcare...

The Issue: Potential for no-flow and leaks under the twist clamp.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2020· CryoLife, Inc.

Recalled Item: CryoValve SG Pulmonary Human Heart Valve. The valve is cryopreserved...

The Issue: On November 10, 2020, it was discovered that there are post- processing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2020· Applied Medical Technology Inc

Recalled Item: AMT Male ENFit-to-Stepped Male (Christmas Tree) Adapter Recalled by Applied...

The Issue: The products subject to this recall may contain obvious, incorrect pouch...

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

Class III — Low RiskOngoing
Medical DeviceNovember 10, 2020· CryoLife, Inc.

Recalled Item: CryoPatch SG Pulmonary Human Cardiac Patch. The patch is cryopreserved...

The Issue: On November 10, 2020, it was discovered that there are post- processing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2020· TissueTech, Inc.

Recalled Item: PROKERA Plus Recalled by TissueTech, Inc. Due to Potential exposure of...

The Issue: Potential exposure of product to microbial contamination.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2020· TissueTech, Inc.

Recalled Item: PROKERA Recalled by TissueTech, Inc. Due to Potential exposure of product to...

The Issue: Potential exposure of product to microbial contamination.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2020· TissueTech, Inc.

Recalled Item: PROKERA Slim Recalled by TissueTech, Inc. Due to Potential exposure of...

The Issue: Potential exposure of product to microbial contamination.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2020· ICU Medical, Inc.

Recalled Item: icumedical Cogent" Hemodynamic Monitoring System - Product Usage: intended...

The Issue: Due to a potential software issue, the display may show the incorrect...

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

Class II — Potential Health HazardOngoing