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. 1,132 recalls have been distributed to Louisiana in the last 12 months.
Showing 2161–2180 of 51,202 recalls
Recalled Item: Crumbled Cookie Bar (85200) Recalled by Rich Ice Cream Co Due to Potential...
The Issue: Potential Listeria Monocytogenes Contamination
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Buffered Penicillin G Potassium for Injection Recalled by Sandoz Inc Due to...
The Issue: Labeling: Label Mix-Up; Some vials of Cefazolin for Injection, USP 1 gram...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cefazolin for Injection Recalled by Sandoz Inc Due to Labeling: Label...
The Issue: Labeling: Label Mix-Up; cartons of Cefazolin for Injection, USP 1 gram were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LYFO-DISK Recalled by Microbiologics Inc Due to KWIK-STIK : 0894P, 0894K and...
The Issue: KWIK-STIK : 0894P, 0894K and LYFO DISK" 0894L may result in failure to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: clomiPRAMINE Hydrochloride Capsules USP 25 mg Recalled by Lupin...
The Issue: Failed Impurities/Degradation Specifications: an out of specification result...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sprinter Cart/Sprinter Cart XL Infusion Pole. Component used to hold...
The Issue: Device does not comply with the labeling requirements of international...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LYFO-DISK Recalled by Microbiologics Inc Due to KWIK-STIK : 0894P, 0894K and...
The Issue: KWIK-STIK : 0894P, 0894K and LYFO DISK" 0894L may result in failure to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RAPIDPoint 500 Systems Wash/Waste Cartridge (4 Pack). Material Number:...
The Issue: Siemens Healthcare Diagnostics is recalling the RAPIDPoint 500 Systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pitavastatin Tablets Recalled by AvKARE Due to Failed Impurity/Degradation...
The Issue: Failed Impurity/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pitavastatin Tablets Recalled by AvKARE Due to Failed Impurity/Degradation...
The Issue: Failed Impurity/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Breathing circuit set Recalled by Hamilton Medical AG Due to Ventilator...
The Issue: Ventilator coaxial breathing circuit may have a crack in blue tubing, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NobelBiocare Tri-Lobe-compatible WP X 6.0mm Engaging Titanium Base Recalled...
The Issue: Engaging titanium base was manufactured 180 degrees around the post from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DxI 800 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: 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: FARAWAVE 1.0 Pulsed Field Ablation Catheter Recalled by Boston Scientific...
The Issue: The potentially impacted units were manufactured using specific equipment...
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: 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: 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: 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.