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. 2,666 recalls have been distributed to Utah in the last 12 months.

49,677 total recalls
2,666 in last 12 months

Showing 14811500 of 28,579 recalls

Medical DeviceJune 12, 2025· Encore Medical, LP

Recalled Item: Brand Name: EMPOWR Dual Mobility" Product Name: EMPOWR Acetabular Recalled...

The Issue: Due to packaging discrepancy with the incorrect tibial inserts/implants...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2025· Encore Medical, LP

Recalled Item: Brand Name: EMPOWR Dual Mobility" Product Name: EMPOWR Acetabular Recalled...

The Issue: Due to packaging discrepancy with the incorrect tibial inserts/implants...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2025· Johnson & Johnson Vision Care, Inc.

Recalled Item: ACUVUE¿ OASYS MAX 1-Day MULTIFOCAL Recalled by Johnson & Johnson Vision...

The Issue: Due to defects (bubbles/voids) identified during standard finished goods testing

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2025· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS Chemistry Products OP Reagent Gen 15. Model Number: 680 Recalled by...

The Issue: Lots from Generation (GEN) 15 of VITROS Chemistry Products OP Reagent may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2025· FUJIFILM Healthcare Americas Corporation

Recalled Item: ASPRIRE Cristalle Mammography System (cleared under K212873) installed with...

The Issue: Devices had an unapproved slabbing software function enabled for use.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2025· CooperSurgical, Inc.

Recalled Item: Endosee System Convenience Kit with IV Tube. Model Number: ES-TRAY-IV....

The Issue: The HSG Procedure Trays and Endosee System Convenience Kits contain...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2025· CooperSurgical, Inc.

Recalled Item: Endosee System Convenience Kit. Model Number: ES-TRAY. Endosee System...

The Issue: The HSG Procedure Trays and Endosee System Convenience Kits contain...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2025· CooperSurgical, Inc.

Recalled Item: HSG Procedure Tray. Model Number: 6050T. The HSG Procedure Tray Recalled by...

The Issue: The HSG Procedure Trays and Endosee System Convenience Kits contain...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2025· RECORDATI RARE DISEASES INC.

Recalled Item: Caphosol Artificial Saliva (32 doses sachet box). 64 x 15 Recalled by...

The Issue: Out of specification stability test result for the Caphosol B solution from...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2025· Boston Foundation For Sight

Recalled Item: BostonSight SCLERAL Lens Recalled by Boston Foundation For Sight Due to...

The Issue: Select orders of lenses were manufactured with errors impacting sagittal...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2025· Boston Foundation For Sight

Recalled Item: BostonSight PROSE Lens. Recalled by Boston Foundation For Sight Due to...

The Issue: Select orders of lenses were manufactured with errors impacting sagittal...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2025· Ortho-Clinical Diagnostics, Inc.

Recalled Item: Brand Name: VITROS Chemistry Products Product Name: VITROS Chemistry...

The Issue: Quality control (QC) drift when certain lots of Performance Verifiers (PVs)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2025· Ortho-Clinical Diagnostics, Inc.

Recalled Item: Brand Name: VITROS Chemistry Products Product Name: VITROS Chemistry...

The Issue: Quality control (QC) drift when certain lots of Performance Verifiers (PVs)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2025· Ortho-Clinical Diagnostics, Inc.

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

The Issue: Quality control (QC) drift when certain lots of Performance Verifiers (PVs)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2025· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS Chemistry Products CHE Slides (Japan) Recalled by Ortho-Clinical...

The Issue: Quality control (QC) drift when certain lots of Performance Verifiers (PVs)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2025· Boston Scientific Corporation

Recalled Item: Torflex Transseptal Guiding Sheath Kit (TFK-M) TF85-32-63-45 TORFLEX 8.5F...

The Issue: Potential for hole in the Tyvek layer of the sterile barrier pouch, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2025· Boston Scientific Corporation

Recalled Item: VersaCross Access Solution (VXSK) Recalled by Boston Scientific Corporation...

The Issue: Potential for hole in the Tyvek layer of the sterile barrier pouch, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2025· Boston Scientific Corporation

Recalled Item: VersaCross RF Wire (VXW). Indicated for creation of an atrial Recalled by...

The Issue: Potential for hole in the Tyvek layer of the sterile barrier pouch, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2025· Boston Scientific Corporation

Recalled Item: VersaCross Transseptal Sheath Kit (VXS) Product Description/IDs VXS0201 VXS...

The Issue: Potential for hole in the Tyvek layer of the sterile barrier pouch, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2025· Boston Scientific Neuromodulation Corporation

Recalled Item: Superion IDS Kit Superion Indirect Decompression System 8MM Recalled by...

The Issue: As a result of a comprehensive product performance review it was determine...

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

Class II — Potential Health HazardOngoing