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. 2,567 recalls have been distributed to Utah in the last 12 months.

49,677 total recalls
2,567 in last 12 months

Showing 1480114820 of 28,579 recalls

Medical DeviceNovember 6, 2018· Deerfield Imaging, Inc.

Recalled Item: IMRIS ORT 300 Recalled by Deerfield Imaging, Inc. Due to Table may drift in...

The Issue: Table may drift in the roll position while in use

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2018· Deerfield Imaging, Inc.

Recalled Item: IMRIS ORT 100 table Recalled by Deerfield Imaging, Inc. Due to Table may...

The Issue: Table may drift in the roll position while in use

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2018· Deerfield Imaging, Inc.

Recalled Item: IMRIS ORT 200 Recalled by Deerfield Imaging, Inc. Due to Table may drift in...

The Issue: Table may drift in the roll position while in use

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2018· COVIDIEN LLC

Recalled Item: 8Fr SAFE GRAD CAT W/Valve (Argyle Suction Catheter Kits with Chimney Valve)...

The Issue: The product was released into commercial distribution while subject to...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2018· Fresenius Medical Care Renal Therapies Group, LLC

Recalled Item: Optiflux F160NR Capillary High Flux Dialyzer Single Use Only Recalled by...

The Issue: Potential for external blood leaks from the dialyzer header

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2018· Bausch & Lomb Surgical, Inc.

Recalled Item: enVista One Piece Hydrophobic Acrylic Intraocular lens - Is indicated...

The Issue: Cosmetic imperfections on the surface of some lenses.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2018· Capintec Inc

Recalled Item: Captus 700 Thyroid Uptake System Recalled by Capintec Inc Due to There is a...

The Issue: There is a potential for the spring arm failure as a result of a broken...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2018· Capintec Inc

Recalled Item: Captus 3000 Thyroid Uptake System Recalled by Capintec Inc Due to There is a...

The Issue: There is a potential for the spring arm failure as a result of a broken...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2018· Baxter Healthcare Corporation

Recalled Item: GEM Coupler Forceps Recalled by Baxter Healthcare Corporation Due to...

The Issue: Potential presence of rust on Coupler Forceps (GEM4183C).

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2018· Stephanix

Recalled Item: STEPHANIX D2RS Digital Dynamic Remote...

The Issue: The firm has detected a potential risk using the command. After releasing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2018· Ascom (US) Inc.

Recalled Item: Ascom Telligence Nurse Call System Recalled by Ascom (US) Inc. Due to There...

The Issue: There is an issue that could cause the Telligence System Gateway II, NGGTWY2...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2018· Virtual Imaging, Inc.

Recalled Item: RadPRO(R) Mobile 40kW Digital X-Ray System - Model: SM-40HF-B-D-C Product...

The Issue: There is a potential for the RadPRO Mobile 40kW Digital X-Ray System Model...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2018· LivaNova USA Inc.

Recalled Item: SORIN Heater-Cooler System 3T 120V~/60Hz Description of product: Recalled by...

The Issue: The firm has become aware that due to a chemical reaction, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2018· ORTHO-CLINICAL DIAGNOSTICS

Recalled Item: VITROS NT-proBNP Reagent Recalled by ORTHO-CLINICAL DIAGNOSTICS Due to The...

The Issue: The firm is extending their previous July 2018 recall to include additional...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2018· ORTHO-CLINICAL DIAGNOSTICS

Recalled Item: VITROS Anti-HBe Reagent Pack Recalled by ORTHO-CLINICAL DIAGNOSTICS Due to...

The Issue: The firm is extending their previous July 2018 recall to include additional...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2018· R & D Systems, Inc.

Recalled Item: Quantikine¿ IVD¿ ELISA Recalled by R & D Systems, Inc. Due to The Human sTfR...

The Issue: The Human sTfR Quantikine IVD ELISA Kit, catalog # DTFR1, lot P180151 was...

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

Class III — Low RiskOngoing
Medical DeviceNovember 1, 2018· ORTHO-CLINICAL DIAGNOSTICS

Recalled Item: VITROS HBeAg Reagent Recalled by ORTHO-CLINICAL DIAGNOSTICS Due to The firm...

The Issue: The firm is extending their previous July 2018 recall to include additional...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2018· Clark Laboratories, Inc. (dba,Trinity Biotech USA)

Recalled Item: ultra2 Genesys Variants Analyzer Recalled by Clark Laboratories, Inc....

The Issue: lack of 510K

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2018· Clark Laboratories, Inc. (dba,Trinity Biotech USA)

Recalled Item: Genesys 2 Reagent Recalled by Clark Laboratories, Inc. (dba,Trinity Biotech...

The Issue: lack of 510K

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2018· Clark Laboratories, Inc. (dba,Trinity Biotech USA)

Recalled Item: Genesys Analytical Column Recalled by Clark Laboratories, Inc. (dba,Trinity...

The Issue: lack of 510K

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

Class II — Potential Health HazardOngoing