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. 2,646 recalls have been distributed to Louisiana in the last 12 months.
Showing 13461–13480 of 51,202 recalls
Recalled Item: Compella Therapy Air Supply Unit Recalled by Baxter Healthcare Corporation...
The Issue: Potential damage to the power cord may cause the power conductors to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOMET TRAUMA A.L.P.S. FIBULA COMPOSITE LOCKING PLATE 8 HOLE Recalled by...
The Issue: Packaging of various implants may not have sufficient adhesion on all sides,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOMET Sports Medicine JUGGERLOC SLOTTED REAMER: [Item # 110010371 Recalled...
The Issue: Packaging of various implants may not have sufficient adhesion on all sides,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOMET TRAUMA Drill Bit Recalled by Biomet, Inc. Due to Packaging of various...
The Issue: Packaging of various implants may not have sufficient adhesion on all sides,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOMET Trauma Recalled by Biomet, Inc. Due to Packaging of various implants...
The Issue: Packaging of various implants may not have sufficient adhesion on all sides,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Compella Bariatric Bed System Recalled by Baxter Healthcare Corporation Due...
The Issue: Potential damage to the power cord may cause the power conductors to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HCG 6 Recalled by Revive Rx LLC dba Revive Rx Pharmacy Due to Non-sterility;...
The Issue: Non-sterility; bacterial contamination identified as Paenibacillus lautus.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Woody's Smokehouse brand Yogurt Raisins Recalled by Lehi Valley Trading Co,...
The Issue: Bags and tubs of yogurt covered raisins contained undeclared peanuts.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: CombiDiagnost R90 1.1 (709031) Recalled by PHILIPS MEDICAL SYSTEMS Due to...
The Issue: While performing a fluoroscopy examination, there is a potential that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CombiDiagnost R90 1.0 (709030) Recalled by PHILIPS MEDICAL SYSTEMS Due to...
The Issue: While performing a fluoroscopy examination, there is a potential that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HUNTLEIGH Disposable intraoperative Probe Recalled by Huntleigh Healthcare...
The Issue: Faceplate may become detached from the probe body.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation 4-11B Recalled by RaySearch America Inc Due to Incorrect source...
The Issue: Incorrect source to skin or surface distance (SSD) calculation may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity m Integrated Reaction Units (IRU) Recalled by Abbott Molecular, Inc....
The Issue: There is potential for the Reaction Vessels (RVs) detaching from the RV cap...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RISE UP RED EDITION Capsules Recalled by Positive Health Due to Undeclared...
The Issue: Marketed Without An Approved NDA/ANDA: Product was found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Favorite Day Carrot cake soft bake cookies Net Wt 8 Recalled by J & M Foods,...
The Issue: Pecans although listed in the Ingredient Statement, was omitted from the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Nextra Hammertoe Correction System 3.5 Middle and 3.2 Proximal Saw Recalled...
The Issue: Proximal end of the driver is oversized in varying degrees, making it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nextra Hammertoe Correction System Driver SKU: NX-DR Orthopedic surgical...
The Issue: Proximal end of the driver is oversized in varying degrees, making it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nextra Hammertoe Correction System 3.5 Middle 3.2 Proximal Kit SKU: Recalled...
The Issue: Proximal end of the driver is oversized in varying degrees, making it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nextra Hammertoe Correction System 4.5 Middle 3.2 Proximal Kit SKU: Recalled...
The Issue: Proximal end of the driver is oversized in varying degrees, making it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nextra Hammertoe Correction System 4.5 Middle and 3.2 Proximal Saw Recalled...
The Issue: Proximal end of the driver is oversized in varying degrees, making it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.