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. 2,431 recalls have been distributed to Louisiana in the last 12 months.
Showing 42241–42260 of 51,202 recalls
Recalled Item: Arriba! 16 oz. Chili Con Queso-Hot Recalled by Riba Foods Inc Due to...
The Issue: Product may contain undeclared wheat.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Salpica 11.5 oz. Recalled by Riba Foods Inc Due to Undeclared Wheat
The Issue: Product may contain undeclared wheat.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Salpica 8 oz. Ballpark Nacho Recalled by Riba Foods Inc Due to Undeclared Wheat
The Issue: Product may contain undeclared wheat.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Salpica 8 oz. Black Bean Nacho Recalled by Riba Foods Inc Due to Undeclared...
The Issue: Product may contain undeclared wheat.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Potassium Chloride Injection Recalled by Baxter Healthcare Corp. Due to...
The Issue: Labeling: Label Error On Declared Strength: Bags of Potassium Chloride 10...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mucinex DM (guaifenesin 600mg and dextromethorphan HBr 30mg) Recalled by...
The Issue: Defective container: A customer complaint revealed the presence of a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sterile powder Vancomycin Hydrochloride for Injection Recalled by Hospira...
The Issue: Correct Labeled Product Mispack: Product tray containing vials was...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: OSSEOTITE Certain 2 Implant Rx only Recalled by Biomet 3i, LLC Due to...
The Issue: Endosseous Dental Implants in contact with a residual machine fluid caused...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSSEOTITE Tapered Certain Implant Rx Only Recalled by Biomet 3i, LLC Due to...
The Issue: Endosseous Dental Implants in contact with a residual machine fluid caused...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Viper LT System Recalled by Becton Dickinson & Co. Due to Potential for...
The Issue: Potential for false positive Chlamydia trachomatis (CT) results and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Breas Vivo 50 Home Care Ventilator Product Usage: Respiratory Care Recalled...
The Issue: Unintended treatment termination could result from a keypad malfunction in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3i T3 Non-Platform Switched Tapered Implant Rx Only Recalled by Biomet 3i,...
The Issue: Endosseous Dental Implants in contact with a residual machine fluid caused...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Licox Brain Tissue Oxygen Monitoring Integra Licox Recon Tissue...
The Issue: Due to a complaint, it was determined that multiple lots of Licox catheters...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADULT Radiotransparent Electrode Recalled by ConMed Corporation Due to...
The Issue: Philips Healthcare made changes to the design of the connection between...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CONMED PEDIATRIC R2 Multifunction Electrodes Recalled by ConMed Corporation...
The Issue: Philips Healthcare made changes to the design of the connection between...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PEDIATRIC Radiotransparent Electrode Recalled by ConMed Corporation Due to...
The Issue: Philips Healthcare made changes to the design of the connection between...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott Healon EndoCoat Ophthalmic Viscosurgical Device 3% sodium hyaluronate...
The Issue: AMO has received complaints where the finger grip dislodged while depressing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADULT Radiotransparent Electrode Recalled by ConMed Corporation Due to...
The Issue: Philips Healthcare made changes to the design of the connection between...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADULT Radiotransparent Electrode Recalled by ConMed Corporation Due to...
The Issue: Philips Healthcare made changes to the design of the connection between...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fisher and Paykel Healthcare (FPH) IW900-Series Infant Warmer Fisher and...
The Issue: Breakage of the nut that secures the heater head in place, which can cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.