Product Recalls in Louisiana
Product recalls affecting Louisiana — including food, drugs, consumer products, medical devices, and vehicles distributed to Louisiana. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,716 recalls have been distributed to Louisiana in the last 12 months.
Showing 1441–1460 of 29,201 recalls
Recalled Item: DxI 600 Access Immunoassay Analyzer W/Spot B Recalled by Beckman Coulter,...
The Issue: Beckman Coulter has identified that the UniCel DxI 600/800 systems with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DxI 800 Access Immunoassay Analyzer W/Spot B Recalled by Beckman Coulter,...
The Issue: Beckman Coulter has identified that the UniCel DxI 600/800 systems with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DxI 600 Access Immunoassay Analyzer W/Dual Gantry Recalled by Beckman...
The Issue: Beckman Coulter has identified that the UniCel DxI 600/800 systems with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UniCel DxI 600 Access Immunoassay Analyzer Recalled by Beckman Coulter, Inc....
The Issue: Beckman Coulter has identified that the UniCel DxI 600/800 systems with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UniCel DxI 800 Access Immunoassay Analyzer Recalled by Beckman Coulter, Inc....
The Issue: Beckman Coulter has identified that the UniCel DxI 600/800 systems with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LVP Primary Administration Set Recalled by Fresenius Kabi USA, LLC Due to...
The Issue: Potential for external cassette leaks
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LVP Blood Products Administration Set Dual-Inlet Recalled by Fresenius Kabi...
The Issue: Potential for external cassette leaks
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PILLAR SA Ti Recalled by Orthofix U.S. LLC Due to A 37 mm implant width...
The Issue: A 37 mm implant width intervertebral body fusion device has a labeling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LVP Primary Administration Set Recalled by Fresenius Kabi USA, LLC Due to...
The Issue: Potential for external cassette leaks
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LVP Primary Administration Set Recalled by Fresenius Kabi USA, LLC Due to...
The Issue: Potential for external cassette leaks
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Preat Recalled by Preat Corp Due to Due to manufacturing error, digital...
The Issue: Due to manufacturing error, digital analog rotational feature is 180 degrees...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: HeartMate Product Name: Mobile Power Unit Recalled by Thoratec...
The Issue: Due to misaligned V-Lock feature on the Mobile Power Unit power cords, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: HeartMate Product Name: Mobile Power Unit Model/Catalog Number:...
The Issue: Due to misaligned V-Lock feature on the Mobile Power Unit power cords, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Automated Impella Controller (AIC) Recalled by Abiomed, Inc. Due to A...
The Issue: A potential issue with the Automated Impella Controller (AIC) not detecting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dual Flat Panel Monitor (DFPM) accessories for HarmonyAIR E-Series Surgical...
The Issue: The DFPM yoke assembly ("yoke assembly") may detach from the spring arm....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dual Flat Panel Monitor (DFPM) accessories for HarmonyAIR A-Series Surgical...
The Issue: The DFPM yoke assembly ("yoke assembly") may detach from the spring arm....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD COR System Software. Model Number: 444829. Recalled by Becton Dickinson &...
The Issue: Potential for functionality issue that supports the Over labeling feature...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Nellcor Bedside SpO2 Patient Monitoring System: Recalled by...
The Issue: Bedside SpO2 Patient Monitoring System alarms not heard/recognized,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinia Recalled by GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING Due to...
The Issue: Unintended radial detector motion may occur during patient setup or during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Varicam Recalled by GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING Due to...
The Issue: Unintended radial detector motion may occur during patient setup or during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.