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. 2,562 recalls have been distributed to Arizona in the last 12 months.
Showing 31301–31320 of 52,339 recalls
Recalled Item: Alka-Seltzer Extra Strength (500 mg Aspirin (NSAID) Recalled by Bayer...
The Issue: Defective Container: Confirmed customer compliant of small holes or cracks...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Alka-Seltzer Original ( 325 mg Aspirin (NSAID) Recalled by Bayer HealthCare...
The Issue: Defective Container: Confirmed customer compliant of small holes or cracks...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dressing Rect L Recalled by Breg Inc Due to They may not have been sealed...
The Issue: They may not have been sealed prior to sterilization. Products with unsealed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 18L6 HD transducer on the ACUSON S Family ultrasound systems Recalled by...
The Issue: When scanning with the 18L6 HD transducer on the ACUSON HELX" Evolution with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...
The Issue: The stability data does not support the product labeled with a 10-year shelf...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...
The Issue: The stability data does not support the product labeled with a 10-year shelf...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...
The Issue: The stability data does not support the product labeled with a 10-year shelf...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Newport Medical HT70 and HT70- Plus Ventilators Recalled by Newport Medical...
The Issue: Medtronic is issuing a voluntary field corrective action for all its...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: If Hip Recalled by Breg Inc Due to They may not have been sealed prior to...
The Issue: They may not have been sealed prior to sterilization. Products with unsealed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...
The Issue: The stability data does not support the product labeled with a 10-year shelf...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...
The Issue: The stability data does not support the product labeled with a 10-year shelf...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...
The Issue: The stability data does not support the product labeled with a 10-year shelf...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...
The Issue: The stability data does not support the product labeled with a 10-year shelf...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...
The Issue: The stability data does not support the product labeled with a 10-year shelf...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMO 25GA Vitrectomy Cutter (Model Number NGP0025) and AMO 20GA Recalled by...
The Issue: Packaging error. 20GA Vitrectomy Cutters may be found in a 25GA package and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...
The Issue: The stability data does not support the product labeled with a 10-year shelf...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...
The Issue: The stability data does not support the product labeled with a 10-year shelf...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dressing Knee/Shldr Recalled by Breg Inc Due to They may not have been...
The Issue: They may not have been sealed prior to sterilization. Products with unsealed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dressing Shldr XL Recalled by Breg Inc Due to They may not have been sealed...
The Issue: They may not have been sealed prior to sterilization. Products with unsealed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dressing M/U XL Recalled by Breg Inc Due to They may not have been sealed...
The Issue: They may not have been sealed prior to sterilization. Products with unsealed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.