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. 2,417 recalls have been distributed to Louisiana in the last 12 months.
Showing 46821–46840 of 51,202 recalls
Recalled Item: 00595201201 Femur CR-FLEX POR FEM B-L Rx Recalled by Zimmer, Inc. Due to...
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00587806126 Patella MICRO POROUS PAT 26MM X 10MM Recalled by Zimmer, Inc....
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00597203109 Articular Surface CR ART SURF 34/STRIPE YEL 09 Recalled by...
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Recalled by Medtronic Inc. Cardiac Rhythm Disease Management Due...
The Issue: Medtronic recently identified an issue with a subset of Consulta¿ CRT-P and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Intermate Infusion Pump. Indicated for the intravenous...
The Issue: Baxter Healthcare Corporation (Baxter) is issuing an Urgent Product Recall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Regional Analgesia Infusor System with Patient Control....
The Issue: Baxter Healthcare Corporation (Baxter) is issuing an Urgent Product Recall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MedStream Programmable Infusion Pump- Implantable for the intrathecal...
The Issue: Miscalibrated Fill Level Sensor may affect dosing level
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Coiled Tube Infusors (Portable Elastomeric Infusion Systems)....
The Issue: Due to an increase in complaints for leaks at the distal male Luer and Luer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: vega sport Recalled by Sequel Naturals Ltd Due to Raw material supplier of...
The Issue: Raw material supplier of the chocolate used for the bar coating had milk...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: vega one Recalled by Sequel Naturals Ltd Due to Raw material supplier of the...
The Issue: Raw material supplier of the chocolate used for the bar coating had milk...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: vega one Recalled by Sequel Naturals Ltd Due to Raw material supplier of the...
The Issue: Raw material supplier of the chocolate used for the bar coating had milk...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: vega sport Recalled by Sequel Naturals Ltd Due to Raw material supplier of...
The Issue: Raw material supplier of the chocolate used for the bar coating had milk...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: vega one Recalled by Sequel Naturals Ltd Due to Raw material supplier of the...
The Issue: Raw material supplier of the chocolate used for the bar coating had milk...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: VECURONIUM Bromide for Injection Recalled by Sagent Pharmaceuticals Inc Due...
The Issue: CGMP Deviations: product was not manufactured under current good...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Excedrin Extra Strength (Acetaminophen 250 mg Recalled by Novartis Consumer...
The Issue: Defective container: products are packaged in pouches which may not have...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Parsel Plus ( US product: Excedrin Tension Headache) (Acetaminophen 500...
The Issue: Defective container: products are packaged in pouches which may not have...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Excedrin Migraine (Acetaminophen 250 mg Recalled by Novartis Consumer Health...
The Issue: Defective container: products are packaged in pouches which may not have...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection Recalled by Hospira Inc. Due to Lack of...
The Issue: Lack of Assurance of Sterility: The product has the potential for solution...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: No Doz Recalled by Novartis Consumer Health Due to Defective container:...
The Issue: Defective container: products are packaged in pouches which may not have...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BD BBL Vancomycin Screen Agar Recalled by Becton Dickinson & Co. Due to...
The Issue: Microbiological identification media may exhibit reduced levels of Vancomycin.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.