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. 1,074 recalls have been distributed to Louisiana in the last 12 months.
Showing 10961–10980 of 29,201 recalls
Recalled Item: Philips Respironics V60 Plus Ventilator Part Number 1138747 - Product...
The Issue: Ventilator may experience potential issues with the backup battery failures:...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Verigene Respiratory Pathogens Flex Nucleic Acid Test (RP Flex) Model...
The Issue: Potential for a false-negative result.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Respironics V60 Ventilator Part Number 1076709 - Product Usage:...
The Issue: Ventilator may experience potential issues with the backup battery failures:...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Respironics V60 Ventilator Part Number DU1053617 - Product Usage:...
The Issue: Ventilator may experience potential issues with the backup battery failures:...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Respironics V60 Plus Ventilator Part Number 1137276 - Product...
The Issue: Ventilator may experience potential issues with the backup battery failures:...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Respironics V60 Ventilator Part Number 1076716 - Product Usage:...
The Issue: Ventilator may experience potential issues with the backup battery failures:...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Respironics V60 Ventilator Part Number 1053613 - Product Usage:...
The Issue: Ventilator may experience potential issues with the backup battery failures:...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Verigene Gram Negative Blood Culture Nucleic Acid Test (BC-GN) Model...
The Issue: Potential for a false-negative result.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6PLUS1 Multilevel Saliva Calibrator Set Cortisol Cortisone in Saliva...
The Issue: Calibrator lots may not meet stability criteria and could result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MassChrom Cortisol Recalled by Chromsystems Instruments & Chemicals GmbH Due...
The Issue: Control lots may not meet stability criteria and could result in increased...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MassChrom Cortisol Recalled by Chromsystems Instruments & Chemicals GmbH Due...
The Issue: Control lots may not meet stability criteria and could result in increased...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PryTime Medical - ER-Reboa Plus Catheter Recalled by Prytime Medical...
The Issue: There is a potential that catheters may have incorrectly marked balloon and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAC VU360 Recalled by GE Healthcare, LLC Due to Incorrect patient...
The Issue: Incorrect patient identification and/or patient demographic errors.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MANI TROCAR KIT 23G S - Product Usage: for use Recalled by Mani, Inc. -...
The Issue: Dimensions of the Luer connector parts out of specification, may cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MANI Infusion Cannula 23G S - Product Usage: for use Recalled by Mani, Inc....
The Issue: Dimensions of the Luer connector parts out of specification, may cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: All EPIQ and Affiniti Ultrasound systems. Model numbers - EPIQ 5G Recalled...
The Issue: The manufacturer has determined that with certain uncommon workflows there...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM 1600 Analyzer - Product Usage: automated Recalled by Siemens...
The Issue: Test Definition scanning may reset custom settings to defaults. When a 2D...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM 1300 Analyzer - Product Usage: automated Recalled by Siemens...
The Issue: Test Definition scanning may reset custom settings to defaults causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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: Evolut (TM) R System. With the following model numbers: a. EVOLUTR-23...
The Issue: Potential for Transcatheter Aortic Valve (TAV) leaflet damage when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.