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. 2,627 recalls have been distributed to Utah in the last 12 months.

49,677 total recalls
2,627 in last 12 months

Showing 86818700 of 28,579 recalls

Medical DeviceDecember 15, 2021· CellEra LLC

Recalled Item: 20500 Vitale Silver calcium Alginate Dressing Ropes Recalled by CellEra LLC...

The Issue: Firm discovered that an incorrect version of the Instructions for Use (IFU)...

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

Class III — Low RiskOngoing
Medical DeviceDecember 15, 2021· CellEra LLC

Recalled Item: 20544 Vitale Silver calcium Alginate Dressings 4x4 Recalled by CellEra LLC...

The Issue: Firm discovered that an incorrect version of the Instructions for Use (IFU)...

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

Class III — Low RiskOngoing
Medical DeviceDecember 15, 2021· CellEra LLC

Recalled Item: 20548 Vitale Silver calcium Alginate Dressings 4x8 Recalled by CellEra LLC...

The Issue: Firm discovered that an incorrect version of the Instructions for Use (IFU)...

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

Class III — Low RiskOngoing
Medical DeviceDecember 14, 2021· Smith & Nephew, Inc.

Recalled Item: Acufex Access Advanced Positioning Kit - indicated for use to Recalled by...

The Issue: Products were shipped to the Global Distribution Center instead of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2021· Collagen Matrix, Inc.

Recalled Item: DuraMatrix-Onlay Collagen Dura Substitute Membrane 4 inches x 5 inches...

The Issue: Outer packaging (outer pouch) is not sealed compromising sterility and...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2021· Collagen Matrix, Inc.

Recalled Item: RESODURA matrix onlay 10.0 cm x 12.5 cm - indicated Recalled by Collagen...

The Issue: Outer packaging (outer pouch) is not sealed compromising sterility and...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2021· Olympus Corporation of the Americas

Recalled Item: OER-Elite Endoscope Reprocessor-for use in cleaning and high-level...

The Issue: The detergent and alcohol tank tubing may have been incorrectly assembled in...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2021· FEMSelect Ltd

Recalled Item: The EnPlace is a single use trans-vaginal pelvic floor repair Recalled by...

The Issue: Certain lots may not have been packaged wth the Channel Tube Limiter.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 10, 2021· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS Chemistry Products VersaTips Recalled by Ortho-Clinical Diagnostics,...

The Issue: The lot has a shape deformity which may lead to a 16% reduction in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 10, 2021· Mallinckrodt Pharmaceuticals Ireland Ltd

Recalled Item: THERAKOS CELLEX Photopheresis Procedural Kit Recalled by Mallinckrodt...

The Issue: This recall was initiated to recover a Dunnage Case, which is a case of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2021· DIXI MEDICAL USA

Recalled Item: The DIXI Medical Microdeep Depth Electrode (Microdeep Depth Electrode or...

The Issue: Potential deformation of the internal packaging (blister pack) could...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2021· DIXI MEDICAL USA

Recalled Item: The DIXI Medical Microdeep Depth Electrode (Microdeep Depth Electrode or...

The Issue: Potential deformation of the internal packaging (blister pack) could...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2021· DIXI MEDICAL USA

Recalled Item: The DIXI Medical Microdeep Depth Electrode (Microdeep Depth Electrode or...

The Issue: Potential deformation of the internal packaging (blister pack) could...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2021· DIXI MEDICAL USA

Recalled Item: The DIXI Medical Microdeep Depth Electrode (Microdeep Depth Electrode or...

The Issue: Potential deformation of the internal packaging (blister pack) could...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2021· DIXI MEDICAL USA

Recalled Item: The DIXI Medical Microdeep Depth Electrode (Microdeep Depth Electrode or...

The Issue: Potential deformation of the internal packaging (blister pack) could...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2021· DIXI MEDICAL USA

Recalled Item: The DIXI Medical Microdeep Depth Electrode (Microdeep Depth Electrode or...

The Issue: Potential deformation of the internal packaging (blister pack) could...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2021· DIXI MEDICAL USA

Recalled Item: The DIXI Medical Microdeep Depth Electrode (Microdeep Depth Electrode or...

The Issue: Potential deformation of the internal packaging (blister pack) could...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2021· DIXI MEDICAL USA

Recalled Item: The DIXI Medical Microdeep Depth Electrode (Microdeep Depth Electrode or...

The Issue: Potential deformation of the internal packaging (blister pack) could...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2021· DIXI MEDICAL USA

Recalled Item: The DIXI Medical Microdeep Depth Electrode (Microdeep Depth Electrode or...

The Issue: Potential deformation of the internal packaging (blister pack) could...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2021· Getinge Usa Sales Inc

Recalled Item: Vaporizer Sevoflurane Maquet Filling Recalled by Getinge Usa Sales Inc Due...

The Issue: A potential chemical degradation of Sevoflurane by Lewis acids (metal oxides...

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

Class I — Serious Health HazardOngoing