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. 2,798 recalls have been distributed to Arizona in the last 12 months.
Showing 3181–3200 of 52,339 recalls
Recalled Item: POTASSIUM CHLORIDE Inj. Recalled by ICU Medical, Inc. Due to Labeling: Label...
The Issue: Labeling: Label Error on Declared Strength. Overwrap labeled as Potassium...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: POTASSIUM CHLORIDE Inj. Recalled by ICU Medical, Inc. Due to Mislabeling
The Issue: Labeling: Label Error on Declared Strength. Cases labeled POTASSIUM CHLORIDE...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Kids by babyganics SPF 50 totally tropical (titanium dioxide 3/5% Recalled...
The Issue: Chemical Contamination
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nelarabine Injection Recalled by Zydus Pharmaceuticals (USA) Inc Due to...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nelarabine Injection Recalled by Zydus Pharmaceuticals (USA) Inc Due to...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Proxima Drape labeled as PACK Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: Potential breach in pouch packaging which could lead to loss of sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proxima Drape labeled as ORTHO TRAUMA CDS Recalled by MEDLINE INDUSTRIES, LP...
The Issue: Potential breach in pouch packaging which could lead to loss of sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proxima Drape labeled as UNIVERSAL DAVINCI ROBOTIC P. Sterile surgical...
The Issue: Potential breach in pouch packaging which could lead to loss of sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proxima Drape labeled as HEAD AND NECK OSIS Recalled by MEDLINE INDUSTRIES,...
The Issue: Potential breach in pouch packaging which could lead to loss of sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proxima Drape labeled as MINOR PACK and LAPAROSCOPY. Sterile surgical drape....
The Issue: Potential breach in pouch packaging which could lead to loss of sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proxima Drape labeled as ENT-PLASTICS PACK. Sterile surgical drape. Recalled...
The Issue: Potential breach in pouch packaging which could lead to loss of sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proxima Drape labeled as DRAPE C-SECTION W/ WINDOW Recalled by MEDLINE...
The Issue: Potential breach in pouch packaging which could lead to loss of sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proxima Drape labeled as FACE LIFT. Sterile surgical drape. Recalled by...
The Issue: Potential breach in pouch packaging which could lead to loss of sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number:...
The Issue: The potential for devices to fail their self-test as a result of prolonged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number:...
The Issue: The potential for devices to fail their self-test as a result of prolonged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number:...
The Issue: The potential for devices to fail their self-test as a result of prolonged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number:...
The Issue: The potential for devices to fail their self-test as a result of prolonged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number:...
The Issue: The potential for devices to fail their self-test as a result of prolonged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number:...
The Issue: The potential for devices to fail their self-test as a result of prolonged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portex Endotracheal Tube Recalled by Smiths Medical ASD, Inc. Due to...
The Issue: Affected devices have a smaller diameter than expected and may potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.