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 43761–43780 of 51,202 recalls
Recalled Item: Red Yeast Rice High Potency Dietary Supplement Recalled by Independent...
The Issue: Marketed Without An Approved NDA/ANDA: Product is being recalled due to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vitamin C (ascorbic acid) Injection Recalled by Flawless Beauty LLC Due to...
The Issue: Marketed Without An Approved NDA/ANDA: Parenteral product is sold over the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Coaxial Micro-Introducer Kit. Greatbatch Part Number/Bard Access Systems...
The Issue: Greatbatch identified that the documentation does not support the five-year...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp Recalled by...
The Issue: Connection issues between the PD transfer set catheter connector and an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revision K Actuator Test Boards sold as replacement parts for Recalled by...
The Issue: 2008-Series Hemodialysis Machines with Revision K Actuator Test Boards may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation software version 4.0.3.4 RayStation is a software system designed...
The Issue: This notice concerns a problem with the computation of ROI voxel volumes for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BG3515-5 US 5mL BioGlue Surgical Adhesive. BioGlue Surgical Adhesive...
The Issue: Serum albumin component monomer failed to meet internally established end of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius 2008T Hemodialysis Machine with Revision K Actuator Test Boards...
The Issue: 2008-Series Hemodialysis Machines with Revision K Actuator Test Boards may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oasis Coil Extension Cable used with Hitachi Oasis MRI System Recalled by...
The Issue: The firm received a complaint stating the Coil Extension Cable accessory...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PediaCare brand DAY & NIGHT Value Pack DAYTIME MULTI-SYMPTOM Cold Recalled...
The Issue: Presence of Precipitate; small amounts of diphenhydramine precipitated out...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PediaCare brand NIGHTTIME MULTI-SYMPTOM Cold Recalled by Prestige Brands...
The Issue: Presence of Precipitate; small amounts of diphenhydramine precipitated out...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Private Selection Chocolate Hazelnut Mascarpone Ice Cream Recalled by Kroger...
The Issue: The firm discovered that the label for two of their products did not declare...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Private Selection Caramel Hazelnut Fudge Truffle Ice Cream Recalled by...
The Issue: The firm discovered that the label for two of their products did not declare...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Baxter Amia Automated PD systems are used in the treatment Recalled by...
The Issue: System error 01779 is produced when the battery cannot be charged due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard¿ Ventralight" ST Mesh with Echo PS" 12"x14" Reorder Number: Recalled by...
The Issue: Pouch holding sterile inflation assembly and inflation adapter may be open...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mar Cor Purification Recalled by Mar Cor Purification Due to Mar Cor...
The Issue: Mar Cor Purification manufactured Central Water Plant (CWP) reverse osmosis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard¿ Ventralight" ST Mesh with Echo PS TM 7"x9" Reorder Recalled by Davol,...
The Issue: Pouch holding sterile inflation assembly and inflation adapter may be open...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard¿ Ventralight" ST Mesh with Echo PS" 4.5" Circle Reorder Recalled by...
The Issue: Pouch holding sterile inflation assembly and inflation adapter may be open...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard¿ Ventralight" ST Mesh with Echo PS" 8" Circle Number: Recalled by...
The Issue: Pouch holding sterile inflation assembly and inflation adapter may be open...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard¿ Ventralight" ST Mesh with Echo PS" 4"x6" Reorder Number: Recalled by...
The Issue: Pouch holding sterile inflation assembly and inflation adapter may be open...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.