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. 1,002 recalls have been distributed to Utah in the last 12 months.

49,677 total recalls
1,002 in last 12 months

Showing 27241–27260 of 49,677 recalls

Medical DeviceJanuary 2, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: IMMULITE ¿ 2000/IMMULITE ¿ 2000 XPi BR-MA (CA15-3) Recalled by Siemens...

The Issue: Concentrations for the level of biotin that does not interfere is not...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: IMMULITE 2000/IMMULITE ¿ 2000 XPi OM-MA (CA125) Recalled by Siemens...

The Issue: Concentrations for the level of biotin that does not interfere is not...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista¿ Thyroid Stimulating Hormone (TSH) Flex¿ reagent cartridge...

The Issue: The concentrations for biotin listed in the non-interfering substances...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: IMMULITE ¿ /IMMULITE 1000 ¿ Gastrin Recalled by Siemens Healthcare...

The Issue: Concentrations for the level of biotin that does not interfere is not...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: IMMULITE ¿ 2000/IMMULITE ¿ 2000 XPi Anti HBc Recalled by Siemens Healthcare...

The Issue: Concentrations for the level of biotin that does not interfere is not...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: IMMULITE ¿ /IMMULITE ¿ 1000 Vitamin B12 Recalled by Siemens Healthcare...

The Issue: Concentrations for the level of biotin that does not interfere is not...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Centaur¿ DHEA-SO4 Recalled by Siemens Healthcare Diagnostics, Inc. Due...

The Issue: The concentrations for biotin listed in the non-interfering substances...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: IMMULITE ¿ /IMMULITE ¿ 1000 OM-MA (CA125) Recalled by Siemens Healthcare...

The Issue: Concentrations for the level of biotin that does not interfere is not...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista¿ Mass Creatine Kinase (MMB) Flex¿ reagent cartridge Recalled...

The Issue: Concentrations for the level of biotin that does not interfere is not...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2018· Stryker Sustainability Solutions

Recalled Item: Stryker Sustainability Solutions Reprocessed BW Lasso 2515 NAV eco Variable...

The Issue: An EEPROM chip error code may occur when the catheters are used with CARTO...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension¿ Free Thyroxine (FT4L) Flex¿ reagent cartridge Recalled by Siemens...

The Issue: The concentrations for biotin listed in the non-interfering substances...

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

Class II — Potential Health HazardOngoing
DrugJanuary 2, 2018· Aurobindo Pharma Ltd.

Recalled Item: Ampicillin and Sulbactam for Injection 1.5 g vial Recalled by Aurobindo...

The Issue: Presence of Particulate Matter: A confirmed customer report was received for...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 28, 2017· DLC Laboratories, Inc

Recalled Item: Earth's Care Eczema Lotion (2% Colloidal Oatmeal) Skin Protectant with...

The Issue: Microbial Contamination of Non-Sterile Products.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 28, 2017· Bard Access Systems Inc.

Recalled Item: PowerPICC Provena Catheters Recalled by Bard Access Systems Inc. Due to...

The Issue: Possible leaks on the 3 Fr. Single lumen and 4 Fr. Dual lumen PowerPICC...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2017· Ormco/Sybronendo

Recalled Item: Elements Obturation Unit (EOU) used with respective Buchanan Heat Pluggers...

The Issue: Buchanan Heat Pluggers will possibly overheat while used with the Elements...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2017· Mako Surgical Corporation

Recalled Item: Makoplasty RIO Standard System Recalled by Mako Surgical Corporation Due to...

The Issue: Communication-connection error.

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

Class II — Potential Health HazardOngoing
DrugDecember 27, 2017· Pharmedium Services, LLC

Recalled Item: Dexamethasone Sodium Phosphate added to 0.9% Sodium Chloride in all...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 27, 2017· Pharmedium Services, LLC

Recalled Item: Bupivacaine HCl in 0.9% Sodium Chloride in all doses Recalled by Pharmedium...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 27, 2017· Pharmedium Services, LLC

Recalled Item: Fentanyl Citrate and Ropivacaine HCl in 0.9% Sodium Chloride in all...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 27, 2017· Pharmedium Services, LLC

Recalled Item: Nicardipine HCl in 0.9% Sodium Chloride in all strengths Recalled by...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund