Product Recalls in Arizona

Product recalls affecting Arizona — including food, drugs, consumer products, medical devices, and vehicles distributed to Arizona. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,582 recalls have been distributed to Arizona in the last 12 months.

52,339 total recalls
2,582 in last 12 months

Showing 2796127980 of 52,339 recalls

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· 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 CEA 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· Roche Diagnostics Corporation

Recalled Item: Roche Acetaminophen assay 03255379160-HAcetaminophen (P) 20767174160- cobas...

The Issue: The previous version of method sheets for the Acetaminophen assay on the...

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 TG Recalled by Siemens Healthcare Diagnostics,...

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¿ Folate (FOL) Recalled by Siemens Healthcare Diagnostics, Inc....

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 TG 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 BR-MA (CA15-3) 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¿ HBc IgM Recalled by Siemens Healthcare Diagnostics, Inc. Due...

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 ¿ 2000/IMMULITE ¿ 2000 XPi 3g Allergy specific IgE Universal Kit...

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¿ Thyroid Stimulating Hormone (TSHL) 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 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
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: Potassium Chloride in 5% Dextrose in all strengths 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: Ephedrine Sulfate Injection in all strengths 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