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. 2,547 recalls have been distributed to Louisiana in the last 12 months.
Showing 19681–19700 of 29,201 recalls
Recalled Item: ELCA Coronary Atherectomy Catheter. Models: 110-001 Recalled by...
The Issue: Spectranetics Corporation announces a voluntary field action for the Turbo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perceval Sutureless Aortic Heart Valve size S Recalled by Sorin Group USA,...
The Issue: Sorin Group USA, Inc. announces a voluntary field action for the Perceval...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Flexible Shaft Recalled by Synthes (USA) Products LLC Due to...
The Issue: Non-conforming material used.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SURESOUND22US Multipack (US Distribution) containing 2 packs of six devices....
The Issue: Breach in sterile barrier compromising product sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natus neoBLUE blanket LED Phototherapy system Recalled by Natus Medical...
The Issue: neoBLUE blanket LED Phototherapy System distributed since release of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gomco Circumcision Clamps with separate O-Ring Component: The device is...
The Issue: Aesculap has received complaints of excessive bleeding after use of Gomco...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Freelite Human Lambda Free Kit for use on SPAPLUS Product Code: LK018.S...
The Issue: A change in the calibration curve causing an increase in false prozone flags.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 12C (AdaPTinsight) Affected component: AdaPTinsight software Product Usage:...
The Issue: IBA is initiating this recall to address an issue identified with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LMA MADgic Recalled by Teleflex Medical Due to Product Defect; These...
The Issue: Product Defect; These products may produce a straight stream instead of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLEXI NOZZLE LONG Recalled by Teleflex Medical Due to Product Defect; These...
The Issue: Product Defect; These products may produce a straight stream instead of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LMA MADomizer Recalled by Teleflex Medical Due to Product Defect; These...
The Issue: Product Defect; These products may produce a straight stream instead of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLEXI NOZZLE SHORT Product Usage: These products are used for Recalled by...
The Issue: Product Defect; These products may produce a straight stream instead of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LMA MADett Recalled by Teleflex Medical Due to Product Defect; These...
The Issue: Product Defect; These products may produce a straight stream instead of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mucosal Atomization Device (MAD) Recalled by Teleflex Medical Due to Product...
The Issue: Product Defect; These products may produce a straight stream instead of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Scientific Solutions Americas Corporation ( OSSA ) Model: VANTA...
The Issue: Possible unintentional x-ray emission after users attempt early termination...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LMA MADdy Recalled by Teleflex Medical Due to Product Defect; These products...
The Issue: Product Defect; These products may produce a straight stream instead of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS CRP Slides: 1) VITROS¿ Chemistry Products CRP Slides (250 Recalled by...
The Issue: CRP samples diluted using VITROS Chemistry Products Specialty Diluent,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Universal Electrosurgical Pad Recalled by 3M Company - Health Care...
The Issue: 3M is recalling Universal Electrosurgical Pads because a report of an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OR Table Recalled by Trumpf Medical Systems, Inc. Due to Trumpf has...
The Issue: Trumpf has identified six incidents of pinched cables.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SONNET Mini Battery Pack CableProduct Usage: The SONNET Mini Battery...
The Issue: Unit Defect: Firm inspection revealed units did not have the compartment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.