Product Recalls in Alabama
Product recalls affecting Alabama — including food, drugs, consumer products, medical devices, and vehicles distributed to Alabama. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,494 recalls have been distributed to Alabama in the last 12 months.
Showing 20941–20960 of 28,641 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: 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: Hill-Rom Bariatric Power Recliner Recalled by Hill-Rom, Inc. Due to The...
The Issue: The recliners were shipped without the foot rest ottoman linkage side...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AGFA Digital Radiography X-Ray System DX-D100 DX-D100 is indicated for...
The Issue: The DX-D100 User Manual already contained information about to move a...
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: 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: HeaterBaum Foot & Ankle Heating Pad Recalled by Ergoactives, Llc Due to...
The Issue: Products are marketed without a cleared 510k.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy 100 Recalled by Philips Respironics Due to Software Issue
The Issue: Software Issue
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.
Recalled Item: 2.3mm Turbo-Power OTW Recalled by Spectranetics Corp. Due to The product is...
The Issue: The product is labeled with an expiration date that is past its shelf life.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OraQuick HCV Visual Panel Intended to assist new operation Recalled by...
The Issue: OraSure Technologies, Inc. discovered the package insert included with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Restoris Multicompartmental Knee (MCK) System RESTORIS MCK is indicated for...
The Issue: Reports where the Mylar/Tyvek pouch for RESTORIS MCK Baseplate in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.