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. 1,930 recalls have been distributed to Arizona in the last 12 months.
Showing 21361–21380 of 29,154 recalls
Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...
The Issue: If excessive pressure is applied to the distal end of the endoscope, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Herga foot switch Recalled by Zimmer Biomet, Inc. Due to Complaints were...
The Issue: Complaints were received reporting the system would freeze/shut down while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...
The Issue: If excessive pressure is applied to the distal end of the endoscope, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...
The Issue: If excessive pressure is applied to the distal end of the endoscope, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...
The Issue: If excessive pressure is applied to the distal end of the endoscope, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...
The Issue: If excessive pressure is applied to the distal end of the endoscope, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeadCare II Blood Lead Test Kit Recalled by Magellan Diagnostics, Inc. Due...
The Issue: LeadCare II Test Kits controls out of range
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...
The Issue: If excessive pressure is applied to the distal end of the endoscope, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...
The Issue: If excessive pressure is applied to the distal end of the endoscope, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...
The Issue: If excessive pressure is applied to the distal end of the endoscope, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...
The Issue: If excessive pressure is applied to the distal end of the endoscope, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...
The Issue: If excessive pressure is applied to the distal end of the endoscope, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...
The Issue: If excessive pressure is applied to the distal end of the endoscope, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...
The Issue: If excessive pressure is applied to the distal end of the endoscope, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...
The Issue: If excessive pressure is applied to the distal end of the endoscope, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...
The Issue: If excessive pressure is applied to the distal end of the endoscope, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CDI H/S Cuvette Recalled by Sorin Group USA, Inc. Due to The CDI System 500...
The Issue: The CDI System 500 monitor displays the "H/S DISCONNECT AT CUVETTE" error...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CEA / CD66e Ab-2 Recalled by Lab Vision Corporation Due to Certain lots of...
The Issue: Certain lots of CEA/CD66e Ab2 were produced with a dilution factor of 1:100...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A Picture Archiving and Communication System (PACS) intended to display...
The Issue: To inform users about the possible incorrect values for Distance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mobile wDR motorized portable diagnostic X-ray systems. Intended for use...
The Issue: This is related to previous 806 Notifications about uncommanded movements of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.