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. 1,160 recalls have been distributed to Arizona in the last 12 months.
Showing 2361–2380 of 52,339 recalls
Recalled Item: Acetaminophen Tablets Recalled by Aurobindo Pharma USA Inc Due to cGMP...
The Issue: cGMP deviations: Due to confirmed consumer complaints received with the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Femoral Nail Recalled by Stryker GmbH Due to Investigation determined that...
The Issue: Investigation determined that one lot of the T2 Greater Trochanter Nail...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Femoral Nail Recalled by Stryker GmbH Due to Investigation determined that...
The Issue: Investigation determined that one lot of the T2 Greater Trochanter Nail...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product: Atellica CH Diluent - CONS 2 x 1.5L Recalled by Siemens Healthcare...
The Issue: Contamination of the diluent by sodium hypochlorite (NaOCl) which may impact...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jewel Precision Reusable Rigid Sterilization Container System. Model/Catalog...
The Issue: The Instructions for Use do not match the 510(k) FDA cleared indications for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IontoPatch 80 Recalled by LTS Therapy Systems, LLC Due to The nonwoven pads...
The Issue: The nonwoven pads in the device do not absorb the saline solution or any...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IontoPatch STAT Recalled by LTS Therapy Systems, LLC Due to The nonwoven...
The Issue: The nonwoven pads in the device do not absorb the saline solution or any...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LUCAS 2 Recalled by Jolife AB Due to Due to demonstration units of chest...
The Issue: Due to demonstration units of chest compression system being provided to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Becton Dickinson Infusion Therapy Systems, Inc. Due to Due to...
The Issue: Due to customer complaints, there is the possibility that catheter needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Becton Dickinson Infusion Therapy Systems, Inc. Due to Due to...
The Issue: Due to customer complaints, there is the possibility that catheter needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Becton Dickinson Infusion Therapy Systems, Inc. Due to Due to...
The Issue: Due to customer complaints, there is the possibility that catheter needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UMOVY ACIDO HIALURONICO Recalled by Umary-USA.com Due to Undeclared Ingredients
The Issue: Marketed without approved NDA/ANDA- Laboratory analysis found product to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: UNAVY ACIDO HIALURONICO Recalled by Umary-USA.com Due to Undeclared Ingredients
The Issue: Marketed without approved NDA/ANDA- Laboratory analysis found product to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nicotinamide adenine dinucleotide (NAD+): 100mg/mL Recalled by Thrive Health...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tirzepatide Injections Recalled by Thrive Health and Wellness, LLC, dba...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Semaglutide/Cyanocobalamin Injectable Recalled by Thrive Health and...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LL Bioboost Injectable Recalled by Thrive Health and Wellness, LLC, dba...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LX Bioboost Plus Recalled by Thrive Health and Wellness, LLC, dba Thrive...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BD Insyte Autoguard Shielded IV Catheter Recalled by Becton Dickinson...
The Issue: Due to customer complaints, there is the possibility that catheter needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Insyte Autoguard Winged Shielded IV Catheter Recalled by Becton Dickinson...
The Issue: Due to customer complaints, there is the possibility that catheter needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.