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. 2,506 recalls have been distributed to Louisiana in the last 12 months.
Showing 27081–27100 of 29,201 recalls
Recalled Item: Synthes Hand Switch - Electric Pen Drive Recalled by Synthes USA HQ, Inc....
The Issue: Synthes received a complaint from a customer in which the Hand Switch for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...
The Issue: Product coatings require 510K approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes...
The Issue: Product coatings require 510K approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIGACLIP¿ Endoscopic Rotating Multiple Clip Applier (ER320) Recalled by...
The Issue: Ethicon Endo-Surgery is initiating a voluntary recall for LIGACLIP¿ 10mm M/L...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIGACLIP¿ Endoscopic Rotating Multiple Clip Applier Convenience Kit (Flex...
The Issue: Ethicon Endo-Surgery is initiating a voluntary recall for LIGACLIP¿ 10mm M/L...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIGACLIP¿ Endoscopic Rotating Multiple Clip Applier (ER320) Recalled by...
The Issue: Ethicon Endo-Surgery is initiating a voluntary recall for LIGACLIP¿ 10mm M/L...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various types of Fetal Bovine Serum Bovine sourced Animal Sera Recalled by...
The Issue: Current product labeling band data sheets state that FBS Pharma Grade and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Curity I.V. Start Kit Recalled by Covidien LLC Due to On March 26, 2013...
The Issue: On March 26, 2013 Covidien received a recall notice from one of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Curity Staple Remover Kit Recalled by Covidien LLC Due to On March 26, 2013...
The Issue: On March 26, 2013 Covidien received a recall notice from one of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BBL DrySlide Oxidase Kit Recalled by Becton Dickinson & Co. Due to In-vitro...
The Issue: In-vitro diagnostic agents were placed into incorrect packaging for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BBL DrySlide PYR Kit Recalled by Becton Dickinson & Co. Due to In-vitro...
The Issue: In-vitro diagnostic agents were placed into incorrect packaging for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...
The Issue: Product coatings require 510K approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rostorelle L Recalled by Coloplast Manufacturing US, LLC Due to Mislabeling
The Issue: Coloplast is recalling one lot of Restorelle L prosthesis because it is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...
The Issue: Product coatings require 510K approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...
The Issue: Product coatings require 510K approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes...
The Issue: Product coatings require 510K approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...
The Issue: Product coatings require 510K approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...
The Issue: Product coatings require 510K approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...
The Issue: Product coatings require 510K approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...
The Issue: Product coatings require 510K approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.