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. 1,897 recalls have been distributed to Arizona in the last 12 months.
Showing 27881–27900 of 29,154 recalls
Recalled Item: bioMerieux BacT/ALERT Control Module Recalled by Biomerieux Inc Due to...
The Issue: The product may mislabel patient information on culture specimen bottles due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux BacT/ALERT Combo Module Recalled by Biomerieux Inc Due to Mislabeling
The Issue: The product may mislabel patient information on culture specimen bottles due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling
The Issue: The product may mislabel patient information on culture specimen bottles due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling
The Issue: The product may mislabel patient information on culture specimen bottles due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling
The Issue: The product may mislabel patient information on culture specimen bottles due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling
The Issue: The product may mislabel patient information on culture specimen bottles due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HX2 Temp Manage SYS 120V The Terumo HX2 Temperature Management Recalled by...
The Issue: Based on a retrospective review of quality data, AC Control boards used in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tested AC Control BD Recalled by Terumo Cardiovascular Systems Corporation...
The Issue: Based on a retrospective review of quality data, AC Control boards used in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling
The Issue: The product may mislabel patient information on culture specimen bottles due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Corometrics Qwik Connect Plus Spiral Electrode- Model #7000AA0 A fetal...
The Issue: Thirty fetal scalp electrodes were found to have an incomplete package seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling
The Issue: The product may mislabel patient information on culture specimen bottles due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling
The Issue: The product may mislabel patient information on culture specimen bottles due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling
The Issue: The product may mislabel patient information on culture specimen bottles due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling
The Issue: The product may mislabel patient information on culture specimen bottles due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling
The Issue: The product may mislabel patient information on culture specimen bottles due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Invivo Corporation Expression MRI Patient Monitoring System. The Expression...
The Issue: Invivo Corporation located at 12151 Research Parkway, Orlando, FL 32826 is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MRT-1504/A4 - Titan X MRI System MRT-30 I0A/5 - Titan Recalled by Toshiba...
The Issue: It was found that there is a problem with the LCD monitor used in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Giraffe and Panda Bag and Mask Resuscitation System The T-piece Recalled by...
The Issue: Oxygen and air wall inlet fittings on the back panel of the resuscitation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare - Giraffe and Panda T-Piece Resuscitation System The Recalled...
The Issue: Oxygen and air wall inlet fittings on the back panel of the resuscitation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The SYMBIONIC LEG is an integrated prosthetic leg for transfemoral Recalled...
The Issue: OSSUR is recalling the Symbionic Leg because it is not recognizing the low...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.