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. 2,759 recalls have been distributed to Arizona in the last 12 months.

52,339 total recalls
2,759 in last 12 months

Showing 72617280 of 29,154 recalls

Medical DeviceNovember 16, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Programmable Diagnostic Computer Recalled by Siemens Medical Solutions USA,...

The Issue: The firm will be performing a software update to address a software error...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2022· ConvaTec, Inc

Recalled Item: ConvaTec AQUACEL Foam Ag Adhesive Recalled by ConvaTec, Inc Due to ConvaTec...

The Issue: ConvaTec are voluntarily recalling a batch of AQUACEL¿ Foam Ag Adhesive 10cm...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2022· Conformis, Inc.

Recalled Item: iTotal Identity Impactor Handle Recalled by Conformis, Inc. Due to Loctite...

The Issue: Loctite thread locker (epoxy) may not have been applied to the screw that is...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2022· Insulet Corporation

Recalled Item: Omnipod 5 Automated Insulin Delivery System Product catalog numbers:...

The Issue: The firm has become aware of an issue with the Omnipod 5 Controller where...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2022· Stryker Medical Division of Stryker Corporation

Recalled Item: Power-PRO 2 Recalled by Stryker Medical Division of Stryker Corporation Due...

The Issue: Cot may experience unintended motion due to damaged cables. Potential risk...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2022· GE Medical Systems, LLC

Recalled Item: Vivid S6 ultrasound. Used in ultrasound imaging and analysis in Recalled by...

The Issue: Potential for batteries that have not been replaced at 2 years, as...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2022· GE Medical Systems, LLC

Recalled Item: Vivid S5 N ultrasound. Not marketed in the US. Used Recalled by GE Medical...

The Issue: Potential for batteries that have not been replaced at 2 years, as...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2022· GE Medical Systems, LLC

Recalled Item: Vivid S5 Ultrasound. Used in ultrasound imaging and analysis in Recalled by...

The Issue: Potential for batteries that have not been replaced at 2 years, as...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2022· GE Medical Systems, LLC

Recalled Item: Vivid i ultrasound. Marketed under the following 510(k) numbers: K033139...

The Issue: Potential for batteries that have not been replaced at 2 years, as...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2022· GE Medical Systems, LLC

Recalled Item: Vivid q ultrasound. Used in ultrasound imaging and analysis in Recalled by...

The Issue: Potential for batteries that have not been replaced at 2 years, as...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2022· GE Medical Systems, LLC

Recalled Item: Vivid q N ultrasound. Not marketed in the US. Used Recalled by GE Medical...

The Issue: Potential for batteries that have not been replaced at 2 years, as...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2022· NuVasive Inc

Recalled Item: X-CORE 2 Ti Core Recalled by NuVasive Inc Due to Potential that insert will...

The Issue: Potential that insert will be unable to disengage from the vertebral body...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2022· GE Medical Systems, LLC

Recalled Item: Vivid S6 N ultrasound. Not marketed in the US. Used Recalled by GE Medical...

The Issue: Potential for batteries that have not been replaced at 2 years, as...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2022· GE Medical Systems, LLC

Recalled Item: Vivid i N ultrasound. Not marketed in the US. Used Recalled by GE Medical...

The Issue: Potential for batteries that have not been replaced at 2 years, as...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2022· Biomerieux Inc

Recalled Item: ETEST CLINICAL AMIKACIN AK 256 US S30 Recalled by Biomerieux Inc Due to As...

The Issue: As the temperature and time out of range was exceeded, product performances...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2022· Biomerieux Inc

Recalled Item: VITEK 2 REAGENT AST-GN80 TEST KIT 20 CARDS Recalled by Biomerieux Inc Due to...

The Issue: As the temperature and time out of range was exceeded, product performances...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2022· Biomerieux Inc

Recalled Item: PPM LOMBARD PRODUCTS TSA 10PLT Recalled by Biomerieux Inc Due to As the...

The Issue: As the temperature and time out of range was exceeded, product performances...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2022· Biomerieux Inc

Recalled Item: VIDAS CLINICAL VIDAS LISTERIA 60T Recalled by Biomerieux Inc Due to As the...

The Issue: As the temperature and time out of range was exceeded, product performances...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2022· Biomerieux Inc

Recalled Item: VIDAS CLINICAL VIDAS HCG 60 TESTS Recalled by Biomerieux Inc Due to As the...

The Issue: As the temperature and time out of range was exceeded, product performances...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2022· Biomerieux Inc

Recalled Item: PPM INDUSTRY COMBOURG CHROMID CARBA US 20 PLT Recalled by Biomerieux Inc Due...

The Issue: As the temperature and time out of range was exceeded, product performances...

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

Class II — Potential Health HazardOngoing