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 21541–21560 of 51,202 recalls
Recalled Item: Endotrac EPF/EGR Push Blade Recalled by Stryker GmbH Due to The seal...
The Issue: The seal integrity of the sterile bag containing the kits may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endintrak 2 Hook Blade Recalled by Stryker GmbH Due to The seal integrity of...
The Issue: The seal integrity of the sterile bag containing the kits may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endotrac EPF/EGR Triangle Blade Recalled by Stryker GmbH Due to The seal...
The Issue: The seal integrity of the sterile bag containing the kits may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endotrac EPF/EGR Hook Blade Recalled by Stryker GmbH Due to The seal...
The Issue: The seal integrity of the sterile bag containing the kits may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endintrak¿ 2 Hook Blade Recalled by Stryker GmbH Due to The seal integrity...
The Issue: The seal integrity of the sterile bag containing the kits may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endotrac ECTR Triangle Blade Recalled by Stryker GmbH Due to The seal...
The Issue: The seal integrity of the sterile bag containing the kits may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endotrac ECTR Push Blade Recalled by Stryker GmbH Due to The seal integrity...
The Issue: The seal integrity of the sterile bag containing the kits may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endotrac ECTR Hook Blade Recalled by Stryker GmbH Due to The seal integrity...
The Issue: The seal integrity of the sterile bag containing the kits may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endotrac EPF/EGR Triangle Blade Recalled by Stryker GmbH Due to The seal...
The Issue: The seal integrity of the sterile bag containing the kits may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endotrac ECTR Hook Blade Recalled by Stryker GmbH Due to The seal integrity...
The Issue: The seal integrity of the sterile bag containing the kits may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endotrac ECTR Triangle Blade Recalled by Stryker GmbH Due to The seal...
The Issue: The seal integrity of the sterile bag containing the kits may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RITZ PRINCESS Recalled by Allergan PLC Due to The action was initiated...
The Issue: The action was initiated following notification by the U.S. FDA of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natrelle 150 Full Height and Short Height Implants Recalled by Allergan PLC...
The Issue: The action was initiated following notification by the U.S. FDA of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McGhan BioDIMENSIONAL silicone-Filled Breast Implants Recalled by Allergan...
The Issue: The action was initiated following notification by the U.S. FDA of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natrelle Inspira Recalled by Allergan PLC Due to The action was initiated...
The Issue: The action was initiated following notification by the U.S. FDA of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natrelle and McGhan Silicone-Filled Breast Implants Recalled by Allergan PLC...
The Issue: The action was initiated following notification by the U.S. FDA of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natrelle 410 Recalled by Allergan PLC Due to The action was initiated...
The Issue: The action was initiated following notification by the U.S. FDA of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natrelle 133 Tissue Expanders (also named style 133 BIOSPAN Tissue Recalled...
The Issue: The action was initiated following notification by the U.S. FDA of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natrelle and McGhan 410 TruForm 2 (Soft Touch) BIOCELL breast implant...
The Issue: The action was initiated following notification by the U.S. FDA of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemospray Endoscopic Hemostat Recalled by Wilson-Cook Medical Inc. Due to...
The Issue: Potential for Hemospray device to be unable to spray powder due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.