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. 2,368 recalls have been distributed to Utah in the last 12 months.

49,677 total recalls
2,368 in last 12 months

Showing 4396143980 of 49,677 recalls

DrugOctober 16, 2013· Taro Pharmaceuticals U.S.A., Inc.

Recalled Item: Ciclopirox Shampoo 1% Recalled by Taro Pharmaceuticals U.S.A., Inc. Due to...

The Issue: Subpotent. drug

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

Class III — Low RiskOngoing
Refund
Medical DeviceOctober 16, 2013· Baxter Healthcare Corp.

Recalled Item: The HomeChoice Pro APD System is a peritoneal dialysis system. Recalled by...

The Issue: The occluder in affected devices 1) may have sharp edges that could cut the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2013· Bausch & Lomb Surgical, Inc.

Recalled Item: Bausch & Lomb AKREOS AO Micro Incision Lens The Akreos Recalled by Bausch &...

The Issue: Lens was manufactured with incorrect raw material.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2013· Microgenics Corp

Recalled Item: Thermo Fisher Scientific/Microgenics brand CEDIA Tobramycin II Assay...

The Issue: Microgenics Corp., part of Thermo Fisher Scientific, is recalling CEDIA...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2013· Cutera, Inc.

Recalled Item: Cutera brand truSculpt infrared System (optional) Recalled by Cutera, Inc....

The Issue: Cutera received two adverse events associated with the edge of the...

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

Class II — Potential Health HazardOngoing
DrugOctober 15, 2013· B. Braun Medical Inc

Recalled Item: Cefepime for Injection USP and Dextrose Injection USP Recalled by B. Braun...

The Issue: Presence of Particulate Matter: The 1g Cefepime for Injection USP and...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 15, 2013· VistaPharm, Inc.

Recalled Item: Phenytoin Oral Suspension USP 125mg/5mL Recalled by VistaPharm, Inc. Due to...

The Issue: Defective Container: A lidding deformity allowed for the product to have out...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 15, 2013· Radiometer America Inc

Recalled Item: ABL90 FLEX Analyzer Radiometer Medical ApS Recalled by Radiometer America...

The Issue: RADIOMETER become aware that if the ABL90 FLEX is tilted, this may...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 15, 2013· Synthes USA HQ, Inc.

Recalled Item: Synthes Material Mix (Adjustable Cervical Distractor-Right Recalled by...

The Issue: One material batch used for production of the affected parts of the Synthes...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 15, 2013· Teleflex Medical

Recalled Item: Green Rusch - Lite Disposable Metal Laryngoscope Ridge Blade to Recalled by...

The Issue: Labeling inconsistency

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2013· Philips Medical Systems, Inc.

Recalled Item: Philips Multi Diagnost Eleva II Recalled by Philips Medical Systems, Inc....

The Issue: The possibility of the Air Kerma Rate for low dose mode will not be reduced...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2013· Philips Medical Systems, Inc.

Recalled Item: Philips Multi Diagnost Eleva with FlatDetector Recalled by Philips Medical...

The Issue: The possibility of the Air Kerma Rate for low dose mode will not be reduced...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2013· Synthes (USA) Products LLC

Recalled Item: Synthes 14.5 mm Outer Protection Sleeve for Suprapatellar Synthes 14.5...

The Issue: Complaints were received reporting that a product packaged as a 14.5 mm...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2013· Philips Healthcare Informatics, Inc.

Recalled Item: Philips brand IntelliSpace PACS 4.4 Recalled by Philips Healthcare...

The Issue: Philips Healthcare became aware of a software problem with the IntelliSpace...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2013· Fresenius Medical Care Holdings, Inc.

Recalled Item: Fresenius Liberty¿ Cycler Part Number: RTLR180111 Product Usage: The Liberty...

The Issue: Fluid leaking may be observed inside the pump compartment of the Liberty...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 13, 2013· Restoration Robotics

Recalled Item: Epsilon Skin Tensioner:Rx Recalled by Restoration Robotics Due to Reports of...

The Issue: Reports of discoloration (residue) on the pins of the skin tensioner have...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 13, 2013· Restoration Robotics

Recalled Item: ARTAS Disposable Kit ( Contains Skin Tensioner FP-45384 Recalled by...

The Issue: Reports of discoloration (residue) on the pins of the skin tensioner have...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 13, 2013· Restoration Robotics

Recalled Item: ARTAS Disposable and Reuseable Kit ( Contains Skin Tensioner FP-45384...

The Issue: Reports of discoloration (residue) on the pins of the skin tensioner have...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 13, 2013· Restoration Robotics

Recalled Item: Sterile Disposable Kit ( Contains Skin Tensioner ASY-25067 Recalled by...

The Issue: Reports of discoloration (residue) on the pins of the skin tensioner have...

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

Class II — Potential Health HazardOngoing
DrugOctober 11, 2013· Teva Pharmaceuticals USA

Recalled Item: Daunorubicin Hydrochloride Injection Recalled by Teva Pharmaceuticals USA...

The Issue: Presence of Precipitate; precipitation of drug product

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

Class II — Potential Health HazardOngoing
Refund