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. 2,092 recalls have been distributed to Arizona in the last 12 months.
Showing 5561–5580 of 29,154 recalls
Recalled Item: Gastroscope-endoscopic ultrasound (EUS) guided fine needle aspiration (FNA)...
The Issue: Channel air drying process was not validated, and that a small percentage of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Insufflation unit Recalled by Olympus Corporation of the Americas Due to...
The Issue: Olympus has become aware of an increased trend of both repairs and customer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tracheal fiberscope-airway management Recalled by Aizu Olympus Co., Ltd. Due...
The Issue: Channel air drying process was not validated, and that a small percentage of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arial Water Resistant Pendant with Wristband Recalled by Securitas...
The Issue: Premature battery depletion presents a risk that alarms will not be received...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arial Water Resistant Pendant with Long Wristband Recalled by Securitas...
The Issue: Premature battery depletion presents a risk that alarms will not be received...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cystonephroscope-endoscopic diagnosis and treatment within the bladder...
The Issue: Channel air drying process was not validated, and that a small percentage of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tracheal videoscope- For airway management Recalled by Aizu Olympus Co.,...
The Issue: Channel air drying process was not validated, and that a small percentage of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arial Water Resistant Pendant with Neck Lanyard Recalled by Securitas...
The Issue: Premature battery depletion presents a risk that alarms will not be received...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transnasal esophagovideoscope-For endoscopy and endoscopic surgery within...
The Issue: Channel air drying process was not validated, and that a small percentage of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hysterovideoscope-For endoscopic diagnosis within the uterus Model Number:...
The Issue: Channel air drying process was not validated, and that a small percentage of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SPRYSTEP VECTOR Recalled by Townsend Design Due to Due to potential air...
The Issue: Due to potential air pockets between layers of material, their is the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SPRYSTEP VECTOR KAFO Recalled by Townsend Design Due to Due to potential air...
The Issue: Due to potential air pockets between layers of material, their is the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CUSTOM SPRYSTEP Recalled by Townsend Design Due to Due to potential air...
The Issue: Due to potential air pockets between layers of material, their is the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DBX Demineralized Bone Matrix Putty 10cc-Indicated for treatment of...
The Issue: Units are labeled as 10cc; however the units have a fill volume of 1cc...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus High-Flow Insufflation Unit Recalled by Olympus Corporation of the...
The Issue: There have been reports of patients suffering arrhythmias, reported as short...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost 4 Flex/Value Recalled by Philips North America Llc Due to...
The Issue: Potential for units suspended on the ceiling to fail and fall.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost C90 Flex/Value/Chest/ER Recalled by Philips North America...
The Issue: Potential for units suspended on the ceiling to fail and fall.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TruDi Navigation System Recalled by Acclarent, Inc. Due to When using...
The Issue: When using affected curette and software, there is a discrepancy between the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost 4 Chest/Emergency Recalled by Philips North America Llc Due...
The Issue: Potential for units suspended on the ceiling to fail and fall.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost C90 High Performance Recalled by Philips North America Llc...
The Issue: Potential for units suspended on the ceiling to fail and fall.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.