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. 2,604 recalls have been distributed to Louisiana in the last 12 months.
Showing 16521–16540 of 29,201 recalls
Recalled Item: Straight Plate Recalled by Orthofix, Inc Due to Firm is conducting a...
The Issue: Firm is conducting a voluntary recall of the Rival Reduce Fracture Plating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CC Plate Recalled by Orthofix, Inc Due to Firm is conducting a voluntary...
The Issue: Firm is conducting a voluntary recall of the Rival Reduce Fracture Plating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EasyTouch (ET) Insulin Syringe 29G 1ml ¿" (Item 829155) Product Recalled by...
The Issue: The retail shelf cartons may be labeled with an incorrect lot number.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: H-Plate Recalled by Orthofix, Inc Due to Firm is conducting a voluntary...
The Issue: Firm is conducting a voluntary recall of the Rival Reduce Fracture Plating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thoratec HeartMate 3 LVAS Implant Kit Recalled by Abbott Due to Reports of...
The Issue: Reports of outflow graft twist occlusions. Patients whose devices experience...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Visaris Vision/Auto Recalled by Visaris DOO Due to A failure of the tube arm...
The Issue: A failure of the tube arm suspension is possible while the tube arm height...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Visaris Vision/Auto Recalled by Visaris DOO Due to A failure of the tube arm...
The Issue: A failure of the tube arm suspension is possible while the tube arm height...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Visaris Vision/Auto Recalled by Visaris DOO Due to A failure of the tube arm...
The Issue: A failure of the tube arm suspension is possible while the tube arm height...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMRIS IMRI 1.5T AND 3T S System Product Usage: The Recalled by Deerfield...
The Issue: The DC power to the IFOSS collision detector control panel at your facility...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Henry Schein CU 1000 Halogen Curing Light Recalled by Handpiece Headquarters...
The Issue: Tip of the curing light was too hot causing a heat sensation in the patients.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CELLSEARCH¿ CIRCULATING Tumor Cell Kits (IVD) (Product Code 7900001)...
The Issue: Unusually high number of total images/unassigned events may require...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Sigma Spectrum Infusion Pump with master Drug Library (Version...
The Issue: Service technician improperly documented final release testing on product,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Sigma Spectrum Infusion Pump with Master Drug Library (Version...
The Issue: Service technician improperly documented final release testing on product,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Sigma Spectrum Infusion Pump with Master Drug Library (Version...
The Issue: Service technician improperly documented final release testing on product,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Sigma Spectrum Infusion Pump with Master Drug Library (Version...
The Issue: Service technician improperly documented final release testing on product,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Sigma Spectrum Infusion Pump with master Drug Library (Version...
The Issue: Service technician improperly documented final release testing on product,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Retractor f/Sciatic Nerve Long Recalled by Synthes (USA) Products LLC Due to...
The Issue: There is a potential for microspores to form on the hollow handle of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Retractor f/Sciatic Nerve Recalled by Synthes (USA) Products LLC Due to...
The Issue: There is a potential for microspores to form on the hollow handle of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Modular Head Component Recalled by Zimmer Biomet, Inc. Due to Two lots of...
The Issue: Two lots of different sized modular heads potentially commingled. Risks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Modular Head Component Recalled by Zimmer Biomet, Inc. Due to Two lots of...
The Issue: Two lots of different sized modular heads potentially commingled. Risks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.