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. 1,122 recalls have been distributed to Arizona in the last 12 months.
Showing 7001–7020 of 29,154 recalls
Recalled Item: Getinge Flow-c Anesthesia System Recalled by Getinge Usa Sales Inc Due to...
The Issue: Due to a software bug, under certain conditions, pressure cannot be built up...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Covera Vascular Covered Stent is a flexible Recalled by Bard Peripheral...
The Issue: An increase in the reported complaint rate for inability to deploy was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydroMID 4Fr Single Lumen Maximal Barrier Kit-indicated for short term...
The Issue: Label with the incorrect component listed on the inner kit Tyvek header bag
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE UNITE FOOT & ANKLE Screw Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: The recall is due to observed intra-operative screw failure. When...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Getinge Flow-e Anesthesia System Recalled by Getinge Usa Sales Inc Due to...
The Issue: Due to a software bug, under certain conditions, pressure cannot be built up...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemopro 2 with Vasoshield Recalled by Maquet Cardiovascular, LLC Due to...
The Issue: Ink on the Vasoshield syringe Maquet logo may chip resulting in an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Luminos Agile with software VC10 - A diagnostic imaging system Recalled by...
The Issue: Potential risk of collision with the ceiling, wall, or objects which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVIS EXERA III Colonovideoscope-For endoscopy and endoscopic surgery within...
The Issue: A single CF-Q180AL colonovideoscope was utilized in a veterinary endoscopy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Luminos Agile Max with software VE10 & VF11- A diagnostic Recalled by...
The Issue: Potential risk of collision with the ceiling, wall, or objects which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Luminos dRF with software VD10- A diagnostic imaging system for Recalled by...
The Issue: Potential risk of collision with the ceiling, wall, or objects which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas SARS-CoV-2 & Influenza A/B Qualitative assay for use on Recalled by...
The Issue: The firm received customer complaints regarding false negative Influenza A...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas SARS-CoV-2 & Influenza A/B Qualitative nucleic acid test for Recalled...
The Issue: The firm received customer complaints regarding false negative Influenza A...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas Influenza A/B & RSV UC (Utility Channel) Qualitative nucleic Recalled...
The Issue: The firm received customer complaints regarding false negative Influenza A...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Uroskop Omnia Max with software VE10 & VF11- A diagnostic Recalled by...
The Issue: Potential risk of collision with the ceiling, wall, or objects which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Luminos dRF Max with software VE10 Recalled by Siemens Medical Solutions...
The Issue: Potential risk of collision with the ceiling, wall, or objects which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RELAY PRO Recalled by Bolton Medical Inc. Due to The product may be shorter...
The Issue: The product may be shorter than packaging indicates
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RELAY PRO Recalled by Bolton Medical Inc. Due to The product may be shorter...
The Issue: The product may be shorter than packaging indicates
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Nuclear Medicine 600/800 series systems Recalled by GE MEDICAL SYSTEMS...
The Issue: A mitigation may not be correctly implemented. If this is the case, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP) Recalled by Datascope...
The Issue: The Cardiosave IABP may shut down unexpectedly due to blood entering in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Rescue Intra-Aortic Balloon Pump (IABP) Recalled by Datascope...
The Issue: The Cardiosave IABP may shut down unexpectedly due to blood entering in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.