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. 2,683 recalls have been distributed to Louisiana in the last 12 months.
Showing 6821–6840 of 29,201 recalls
Recalled Item: Agilent Resolution ctDx FIRST Sample Collection Kit Recalled by AGILENT...
The Issue: Distributed sample collection kit with an unapproved instruction for use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Raystation treatment planning system for radiation therapy Recalled by...
The Issue: It is possible to set a non-zero collimator angle in the Virtual Simulation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFINITY Occipitocervical Upper Thoracic System Recalled by Medtronic...
The Issue: Incorrect type of titanium was used which reduces the gripping strength of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFINITY Occipitocervical Upper Thoracic System Recalled by Medtronic...
The Issue: Incorrect type of titanium was used which reduces the gripping strength of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFINITY Occipitocervical Upper Thoracic System Recalled by Medtronic...
The Issue: Incorrect type of titanium was used which reduces the gripping strength of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFINITY Occipitocervical Upper Thoracic System Recalled by Medtronic...
The Issue: Incorrect type of titanium was used which reduces the gripping strength of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFINITY Occipitocervical Upper Thoracic System Recalled by Medtronic...
The Issue: Incorrect type of titanium was used which reduces the gripping strength of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FoundationOne Companion Diagnostic (F1CDx) Recalled by Foundation Medicine,...
The Issue: An incorrect negative claim was identified on the claims page; the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flex-Neck Catheter External Repair Kit LOT CE-1400/A Recalled by Merit...
The Issue: Product that was built for design verification testing was inadvertently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Attune Revision Limb Preservation System (LPS) Tibial Insert XXSM 18MM...
The Issue: The subject product lots are being recalled because they received a higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Attune Revision Limb Preservation System (LPS) Tibial Insert SM 12MM...
The Issue: The subject product lots are being recalled because they received a higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Attune Revision Limb Preservation System (LPS) Tibial Insert XSM 12MM...
The Issue: The subject product lots are being recalled because they received a higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Attune Revision Limb Preservation System (LPS) Tibial Insert XSM 26MM...
The Issue: The subject product lots are being recalled because they received a higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Attune Posterior (PS) Fixed Bearing (FB) Tibial Insert SZ5 7MM Recalled by...
The Issue: The subject product lots are being recalled because they received a higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis MedStation ES AUX Tower BD Pyxis Recalled by CareFusion 303, Inc....
The Issue: Due to an increase in complaints of door latch assembly failures that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KLS martin Group KLS E-COUPLING ADAPTER E-Coupling Adapter Recalled by...
The Issue: Incorrect Unique Device Identifier/GTIN code was used on product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edward Lifesciences Recalled by Edwards Lifesciences, LLC Due to There is a...
The Issue: There is a potential that the distal end of the catheter may be bent beyond...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edward Lifesciences Recalled by Edwards Lifesciences, LLC Due to There is a...
The Issue: There is a potential that the distal end of the catheter may be bent beyond...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DDU-100 Lifeline Automated External Defibrillator (AED)-Indicated for use on...
The Issue: A component of a sub-assembly used in the affected AEDs had not undergone...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clariti 1-day toric soft contact lenses Recalled by CooperVision, Inc. Due...
The Issue: The lenses manufactured in the affected lot were made with a misaligned axis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.