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 981–1000 of 52,339 recalls
Recalled Item: Brand Name: EDAN Product Name: Vital Signs Monitor Model/Catalog Number:...
The Issue: As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: EDAN Product Name: Fetal Monitor Model/Catalog Number: F2...
The Issue: As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bromocriptine Mesylate Capsules Recalled by Zydus Pharmaceuticals (USA) Inc...
The Issue: Failed Impurities/Degradation Specifications: Out of Specification (OOS)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cardiosave Rescue Recalled by Datascope Corp. Due to The IFU addendum...
The Issue: The IFU addendum updates the Vibration and Shock Table to the correct standards.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Hybrid Recalled by Datascope Corp. Due to The IFU addendum...
The Issue: The IFU addendum updates the Vibration and Shock Table to the correct standards.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Kiestra" Isolate Suspension Cuvette Array Recalled by Becton Dickinson &...
The Issue: The 2D barcodes on these cuvettes contain formatting errors that prevent the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: clomiPRAMINE Hydrochloride Recalled by Zydus Pharmaceuticals (USA) Inc Due...
The Issue: cGMP deviations: an observed Out of Specification of Nitrosamine Drug...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: clomiPRAMINE Hydrochloride Recalled by Zydus Pharmaceuticals (USA) Inc Due...
The Issue: cGMP deviations: an observed Out of Specification of Nitrosamine Drug...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: clomiPRAMINE Hydrochloride Recalled by Zydus Pharmaceuticals (USA) Inc Due...
The Issue: cGMP deviations: an observed Out of Specification of Nitrosamine Drug...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Olympus Thunderbeat Recalled by Olympus Corporation of the Americas Due to...
The Issue: Firm is initiating a removal due to continued reports of adverse events.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Thunderbeat Recalled by Olympus Corporation of the Americas Due to...
The Issue: Firm is initiating a removal due to continued reports of adverse events.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Thunderbeat Recalled by Olympus Corporation of the Americas Due to...
The Issue: Firm is initiating a removal due to continued reports of adverse events.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Thunderbeat 5 mm Recalled by Olympus Corporation of the Americas Due...
The Issue: Firm is initiating a removal due to continued reports of adverse events.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Thunderbeat Recalled by Olympus Corporation of the Americas Due to...
The Issue: Firm is initiating a removal due to continued reports of adverse events.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Thunderbeat 5 mm Recalled by Olympus Corporation of the Americas Due...
The Issue: Firm is initiating a removal due to continued reports of adverse events.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Thunderbeat Recalled by Olympus Corporation of the Americas Due to...
The Issue: Firm is initiating a removal due to continued reports of adverse events.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Thunderbeat 5 mm Recalled by Olympus Corporation of the Americas Due...
The Issue: Firm is initiating a removal due to continued reports of adverse events.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioFire Respiratory Panel 2.1 Recalled by BioFire Diagnostics, LLC Due to...
The Issue: Due to unintended movement of pouch chemistry, nucleic acid test may result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Thunderbeat Recalled by Olympus Corporation of the Americas Due to...
The Issue: Firm is initiating a removal due to continued reports of adverse events.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Thunderbeat 5 mm Recalled by Olympus Corporation of the Americas Due...
The Issue: Firm is initiating a removal due to continued reports of adverse events.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.