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. 2,424 recalls have been distributed to Louisiana in the last 12 months.
Showing 44541–44560 of 51,202 recalls
Recalled Item: XZONE GOLD Recalled by Schindele Enterprises dba Midwest Wholesale Due to...
The Issue: Marketed Without an Approved NDA/ANDA: These dietary supplements contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ExtenZe 600 mg Recalled by Schindele Enterprises dba Midwest Wholesale Due...
The Issue: Marketed Without an Approved NDA/ANDA: These dietary supplements contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BOOST ULTRA Recalled by Schindele Enterprises dba Midwest Wholesale Due to...
The Issue: Marketed Without an Approved NDA/ANDA: These dietary supplements contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: XZEN PLATINUM Recalled by Schindele Enterprises dba Midwest Wholesale Due to...
The Issue: Marketed Without an Approved NDA/ANDA: These dietary supplements contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MiracleZEN Platinum Recalled by Schindele Enterprises dba Midwest Wholesale...
The Issue: Marketed Without an Approved NDA/ANDA: These dietary supplements contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Magic For Men Recalled by Schindele Enterprises dba Midwest Wholesale Due to...
The Issue: Marketed Without an Approved NDA/ANDA: These dietary supplements contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Aminosyn 3.5% M Sulfite-Free Recalled by Hospira Inc. Due to Lack of...
The Issue: Lack of Assurance of Sterility; potential leakage from administrative port.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Heparin Sodium 2000 USP Heparin Units per 1000 mL (2 Recalled by Hospira...
The Issue: Lack of Assurance of Sterility; potential leakage from administrative port.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VITROS Chemistry Products White Slides Recalled by Ortho-Clinical...
The Issue: An incorrect assay value (0.3785) was printed on the product carton for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew RENASYS-AB Abdominal Dressing Kit with Soft Port Recalled by...
The Issue: Reports of wound fluid and /or blood that were not evacuated from beneath...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew RENASYS Soft Port (The RENASYS Recalled by Smith & Nephew...
The Issue: Reports of wound fluid and /or blood that were not evacuated from beneath...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew RENASYS-F Foam Dressing Kit with Soft Port REF #'s: 66800794...
The Issue: Reports of wound fluid and /or blood that were not evacuated from beneath...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew RENASYS-G Sterile Recalled by Smith & Nephew Inc. Due to...
The Issue: Reports of wound fluid and /or blood that were not evacuated from beneath...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew RENASYS-Gauze with Soft Port Kit REF #'s: 66800933 Recalled...
The Issue: Reports of wound fluid and /or blood that were not evacuated from beneath...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew RENASYS-F XL with Soft Port REF #: Recalled by Smith & Nephew...
The Issue: Reports of wound fluid and /or blood that were not evacuated from beneath...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Restoris Multicompartmental Knee (MCK) System is an implant system designed...
The Issue: The product may be mislabeled and could result in the incorrect implant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Model 7305- Mosaic Aortic Obturator The Mosaic Aortic Recalled...
The Issue: Medtronic, Inc. initiated a recall of Medtronic Mosaic Aortic Obturator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ANSPACH Cutting bur Recalled by The Anspach Effort, Inc. Due to Anspach...
The Issue: Anspach product code L-3SD contained product code S-3SD which is shorter in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Panaroma Central Station Product Usage: This device can view real time...
The Issue: Mindray has identified two issues with the Panorama Central Station. Full...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CELLTRACKS ANALYZER II¿ (Product Code 9555) Product Usage: The CELLTRACKS...
The Issue: Janssen Diagnostics, LLC received complaints of camera failures on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.