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. 2,732 recalls have been distributed to Arizona in the last 12 months.
Showing 10981–11000 of 29,154 recalls
Recalled Item: Box Label: ION Fully Articulating Catheter Recalled by Intuitive Surgical,...
The Issue: The distal tip ring of the fully articulating catheter may become dislodged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titan Pump - Product Usage: indicated for male patients suffering Recalled...
The Issue: Potential increased occurrence of pump fracture over the lifetime of the device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mako Integrated Cutting System (MICS) Handpiece Recalled by Mako Surgical...
The Issue: Stryker has discovered a characterization issue associated with the Mako...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fixed Core Wire Guide Recalled by Cook Inc. Due to Affected product was...
The Issue: Affected product was dropped during manufacturing, which may result in a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee floor Recalled by Siemens Medical Solutions USA, Inc Due to Some...
The Issue: Some electronic components within the generator were equipped with an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ViewRay MRIdian System: Model No. 10000 Recalled by Viewray, Inc. Due to...
The Issue: There is a potential that components of the receive coil can reach elevated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ViewRay MRIdian Linac System: Model No. 20000 Recalled by Viewray, Inc. Due...
The Issue: There is a potential that components of the receive coil can reach elevated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Geistlich Bio-Oss Pen 1-2mm 0.5g - Product Usage: natural bone Recalled by...
The Issue: Difficult to expel Geistlich Bio-Oss granules from the pen, resistance could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEVION S250i Recalled by Mevion Medical Systems, Inc. Due to Treatment beam...
The Issue: Treatment beam information disappears on Treatment Console screen while beam...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Geistlich Bio-Oss Pen 0.25-1mm 0.5g - Product Usage: natural bone Recalled...
The Issue: Difficult to expel Geistlich Bio-Oss granules from the pen, resistance could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Geistlich Bio-Oss Pen 0.25-1mm 0.25g - Product Usage: natural bone Recalled...
The Issue: Difficult to expel Geistlich Bio-Oss granules from the pen, resistance could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DABRA Laser (RA-308 Excimer Laser) Intended Use: For use in Recalled by Ra...
The Issue: Due to footswitch not meeting required specification for protection from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Ultrasound Endoscope Recalled by Olympus Corporation of the Americas...
The Issue: A new inspection step was added to the cleaning and disinfection section of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Ultrasound Endoscope Recalled by Olympus Corporation of the Americas...
The Issue: A new inspection step was added to the cleaning and disinfection section of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Ultrasound Endoscope Recalled by Olympus Corporation of the Americas...
The Issue: A new inspection step was added to the cleaning and disinfection section of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Ultrasound Endoscope Recalled by Olympus Corporation of the Americas...
The Issue: A new inspection step was added to the cleaning and disinfection section of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Ultrasound Endoscope Recalled by Olympus Corporation of the Americas...
The Issue: A new inspection step was added to the cleaning and disinfection section of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Ultrasound Endoscope Recalled by Olympus Corporation of the Americas...
The Issue: A new inspection step was added to the cleaning and disinfection section of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Ultrasound Endoscope Recalled by Olympus Corporation of the Americas...
The Issue: A new inspection step was added to the cleaning and disinfection section of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Ultrasound Endoscope Recalled by Olympus Corporation of the Americas...
The Issue: A new inspection step was added to the cleaning and disinfection section of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.