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. 2,425 recalls have been distributed to Utah in the last 12 months.

49,677 total recalls
2,425 in last 12 months

Showing 3600136020 of 49,677 recalls

Medical DeviceNovember 19, 2015· Biomerieux

Recalled Item: Etest¿ PIP/TAZO/CON-4 PTC 256 -pack of 30 tests US. Etest¿ Recalled by...

The Issue: Due to the potential for reporting erroneous results for...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 19, 2015· Biomerieux

Recalled Item: Etest¿ PIP/TAZO/CON-4 PTC 256 - Foam of 100 tests WW. Recalled by Biomerieux...

The Issue: Due to the potential for reporting erroneous results for...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 19, 2015· Boston Scientific Corporation

Recalled Item: Boston Scientific Recalled by Boston Scientific Corporation Due to Boston...

The Issue: Boston Scientific is voluntarily recalling its Chariot" Guiding Sheath. To...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 19, 2015· Biomerieux

Recalled Item: Etest¿ Piperacillin/tazobactam (4 ug/mL) PTc0.016-256-pack of 30 tests WW...

The Issue: Due to the potential for reporting erroneous results for...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 18, 2015· Radiometer America Inc

Recalled Item: TCM CombiM Modules 903-111 Recalled by Radiometer America Inc Due to...

The Issue: Radiometer America, Inc. is recalling TCM CombiM on rare occasions they may...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2015· Mevion Medical Systems, Inc.

Recalled Item: MEVION S250 Radiation therapy system Recalled by Mevion Medical Systems,...

The Issue: The treatment table positioning belt can slip gear positions, resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: Software version VD10E for Syngo X-Workplace Recalled by Siemens Medical...

The Issue: Potential post-processing software issue when using tabcard "4D" on...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2015· Rainbow Specialty & Health Products

Recalled Item: Dressol-X Recalled by Rainbow Specialty & Health Products Due to Rainbow...

The Issue: Rainbow Specialty & Health Products initiated a field action for Dressol-X...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2015· Hardy Diagnostics

Recalled Item: FB Broth Recalled by Hardy Diagnostics Due to The firm is recalling FB Broth...

The Issue: The firm is recalling FB Broth Cat. no. K31, Lot no. 15231 because of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2015· Rainbow Specialty & Health Products

Recalled Item: Dressit-X Recalled by Rainbow Specialty & Health Products Due to Rainbow...

The Issue: Rainbow Specialty & Health Products initiated a field action for Dressol-X...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2015· Owens & Minor Distribution, Inc.

Recalled Item: MediChoice Cohesive Bandages Recalled by Owens & Minor Distribution, Inc....

The Issue: MediChoice sterile cohesive bandages imported and sold under a private brand...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2015· Owens & Minor Distribution, Inc.

Recalled Item: MediChoice Cohesive Bandages Recalled by Owens & Minor Distribution, Inc....

The Issue: MediChoice sterile cohesive bandages imported and sold under a private brand...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2015· Owens & Minor Distribution, Inc.

Recalled Item: MediChoice Cohesive Bandages Recalled by Owens & Minor Distribution, Inc....

The Issue: MediChoice sterile cohesive bandages imported and sold under a private brand...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2015· Biomet, Inc.

Recalled Item: Biomet Integral Centralizer Hip System Recalled by Biomet, Inc. Due to PMMA...

The Issue: PMMA is listed as a material on the label but the product does not contain PMMA.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2015· Becton Dickinson & Company

Recalled Item: BD Vacutainer K2 EDTA (K2E) 5.4mg Plus Blood Collection Tubes. Recalled by...

The Issue: Some tubes were manufactured with the stopper not fully inserted into the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2015· Olympus Corporation of the Americas

Recalled Item: Olympus ENDOEYE HD II Video Telescopes. Models WA50040A ENDOEYE HD II...

The Issue: A damaged temperature sensor at the ENDOEYE tip caused the distal end to...

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

Class II — Potential Health HazardOngoing
FoodNovember 16, 2015· The Kroger Co

Recalled Item: BAKERY FRESH GOODNESS Chocolate Brownie NET WT 16 OZ (1 LB) 453 g CONTAINS:...

The Issue: The firm was notified by a consumer of undeclared walnuts in the product.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodNovember 16, 2015· Thrive Foods LLC

Recalled Item: Organic blenditup Protein + Plant Based Smoothie Mix Recalled by Thrive...

The Issue: Product adulterated. End user found a wingnut inside their canister; the...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 16, 2015· Nephron Pharmaceuticals Corp.

Recalled Item: Sodium Chloride Inhalation Solution Recalled by Nephron Pharmaceuticals...

The Issue: Lack of Assurance of Sterility: Internal dye ingress test failure to assure...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 16, 2015· Nephron Pharmaceuticals Corp.

Recalled Item: Sodium Chloride Inhalation Solution Recalled by Nephron Pharmaceuticals...

The Issue: Lack of Assurance of Sterility: Internal dye ingress test failure to assure...

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

Class II — Potential Health HazardOngoing