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. 2,678 recalls have been distributed to Louisiana in the last 12 months.

51,202 total recalls
2,678 in last 12 months

Showing 73017320 of 51,202 recalls

Medical DeviceNovember 15, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Centurion Kits Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: Medline Industries, LP is recalling certain kits and trays that were...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceNovember 15, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE Kits Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Medline...

The Issue: Medline Industries, LP is recalling certain kits and trays that were...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceNovember 15, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Centurion Kits Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: Medline Industries, LP is recalling certain kits and trays that were...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceNovember 15, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE BRONCHOSCOPY TRAY Recalled by MEDLINE INDUSTRIES, LP - Northfield...

The Issue: Medline Industries, LP is recalling certain kits and trays that were...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceNovember 15, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE ARTERIAL BUNDLE NO CATHETER Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Medline Industries, LP is recalling certain kits and trays that were...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceNovember 15, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE kits and trays Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...

The Issue: Medline Industries, LP is recalling certain kits and trays that were...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceNovember 15, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE Kits Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Medline...

The Issue: Medline Industries, LP is recalling certain kits and trays that were...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceNovember 15, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Kits Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Medline...

The Issue: Medline Industries, LP is recalling certain kits and trays that were...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceNovember 15, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Centurion Kits Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: Medline Industries, LP is recalling certain kits and trays that were...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceNovember 15, 2023· Canon Medical System, USA, INC.

Recalled Item: The INFX-8000F is designed to take advantage of the latest Recalled by Canon...

The Issue: VAREX changed the manufacturing of the internal board, and the detectors...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2023· Canon Medical System, USA, INC.

Recalled Item: The device is an X-ray system that is capable of Recalled by Canon Medical...

The Issue: VAREX changed the manufacturing of the internal board, and the detectors...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2023· Medtronic MiniMed, Inc.

Recalled Item: Guardian 4 Glucose Sensor Recalled by Medtronic MiniMed, Inc. Due to Some...

The Issue: Some sensors may have a glucose oxidase (GOX) layer thickness outside of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2023· SoClean, Inc

Recalled Item: SoClean 2 Recalled by SoClean, Inc Due to New User Manual with additional...

The Issue: New User Manual with additional instructions for use and a hose and mask...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2023· SoClean, Inc

Recalled Item: SoClean 3 Recalled by SoClean, Inc Due to New User Manual with additional...

The Issue: New User Manual with additional instructions for use and a hose and mask...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2023· Baxter Healthcare Corporation

Recalled Item: Baxter Amia Automated Peritoneal Dialysis (APD) Cycler Set Recalled by...

The Issue: There is to an increase in complaints related to failure alarms for Wet...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2023· C.R. Bard Inc

Recalled Item: Sensica Urine Output System Recalled by C.R. Bard Inc Due to BD (C.R. Bard)...

The Issue: BD (C.R. Bard) has received user complaints reporting that when the device...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2023· Spectranetics Corporation

Recalled Item: Spectranetics Turbo-Elite Laser Atherectomy Catheter 2.0 RX Spectranetics...

The Issue: Incorrect product labeling. Exterior product box label does not match...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugNovember 14, 2023· Baxter Healthcare Corporation

Recalled Item: Ondansetron Injection Recalled by Baxter Healthcare Corporation Due to...

The Issue: Failed pH Specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 14, 2023· Bard Peripheral Vascular Inc

Recalled Item: BD Recanalization System Recalled by Bard Peripheral Vascular Inc Due to...

The Issue: Recanalization systems may be in a manufacturing mode that allows the system...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2023· Maquet Medical Systems USA

Recalled Item: CARDIOHELP-i Heart Lung Support System: Blood oxygenation and carbon dioxide...

The Issue: CARDIOHELP-i System was not properly tested to measure leakage current

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing