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. 2,696 recalls have been distributed to Louisiana in the last 12 months.

51,202 total recalls
2,696 in last 12 months

Showing 46014620 of 29,201 recalls

Medical DeviceFebruary 23, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Centurion manual surgical kits labeled as: a) SUTURE REMOVAL TRAY Recalled...

The Issue: Product may have a weak seal which may result in a breach of sterility of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Centurion DISP.UMBILICAL CORD CLAMP CUTTER(CTR300) Recalled by MEDLINE...

The Issue: Product may have a weak seal which may result in a breach of sterility of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Centurion manual surgical kits labeled as: a) ST. VIRTUS SPLINTER Recalled...

The Issue: Product may have a weak seal which may result in a breach of sterility of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Centurion Manual surgical kits labeled as: a) 15ML SAMPLING TUBE WITH CAP...

The Issue: Product may have a weak seal which may result in a breach of sterility of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Centurion Curette kits labeled as: a) STERILE BUCK EAR CURETTE "00" (25697)...

The Issue: Product may have a weak seal which may result in a breach of sterility of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Centurion scalpel handle kits labeled as: a) STERILE # 3 SCALPEL HANDLE...

The Issue: Product may have a weak seal which may result in a breach of sterility of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2024· Siemens Medical Solutions USA, Inc.

Recalled Item: ACUSON Maple Diagnostic Ultrasound System Recalled by Siemens Medical...

The Issue: On ultrasound systems, when Cardiac DICOM SR feature is configured to...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2024· CareFusion 303, Inc.

Recalled Item: BD Pyxis MedStation 4000 . Intended to securely store Recalled by CareFusion...

The Issue: Retroactive-Due to increase in complaints, their is a potential for drawer...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2024· CareFusion 303, Inc.

Recalled Item: BD Pyxis MedStation Auxiliary 4000 . Intended to securely Recalled by...

The Issue: Retroactive-Due to increase in complaints, their is a potential for drawer...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2024· Siemens Medical Solutions USA, Inc.

Recalled Item: ACUSON Juniper Diagnostic Ultrasound System Recalled by Siemens Medical...

The Issue: On ultrasound systems, when Cardiac DICOM SR feature is configured to...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2024· Magellan Diagnostics, Inc.

Recalled Item: The LeadCare¿ II Blood Lead Test System relies on electrochemistry Recalled...

The Issue: Calibration Buttons being used in the kitting process were incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2024· CareFusion 303, Inc.

Recalled Item: BD Pyxis MedStation ES (Med ES Main) . Intended Recalled by CareFusion 303,...

The Issue: Retroactive-Due to increase in complaints, their is a potential for drawer...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2024· CareFusion 303, Inc.

Recalled Item: BD Pyxis MedStation Auxiliary ES . Intended to securely Recalled by...

The Issue: Retroactive-Due to increase in complaints, their is a potential for drawer...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2024· Siemens Medical Solutions USA, Inc.

Recalled Item: ACUSON Redwood 1.0 Diagnostic Ultrasound System Recalled by Siemens Medical...

The Issue: On ultrasound systems, when Cardiac DICOM SR feature is configured to...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2024· Baxter Healthcare Corporation

Recalled Item: Surgical Tools and Cardiovascular Specialty marketing brochures Recalled by...

The Issue: The Surgical Tools and Cardiovascular Specialty marketing brochures...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2024· Baxter Healthcare Corporation

Recalled Item: Surgical Tools and Cardiovascular Specialty marketing brochures Recalled by...

The Issue: The Surgical Tools and Cardiovascular Specialty marketing brochures...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2024· Bolton Medical Inc.

Recalled Item: RELAY PRO Thoracic Stent-Graft System Recalled by Bolton Medical Inc. Due to...

The Issue: The stent-graft inside the delivery system was the incorrect size.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2024· Baxter Healthcare Corporation

Recalled Item: Surgical Tools and Cardiovascular Specialty marketing brochures Recalled by...

The Issue: The Surgical Tools and Cardiovascular Specialty marketing brochures...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2024· Covidien

Recalled Item: Situate Laparotomy Sponge Recalled by Covidien Due to Packs including 5...

The Issue: Packs including 5 laparotomy sponges may contain incorrect product with a...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2024· Alcon Research, LLC

Recalled Item: SYRINGE Recalled by Alcon Research, LLC Due to Medline Bulb irrigation...

The Issue: Medline Bulb irrigation syringes recalled due to potential for packaging...

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

Class II — Potential Health HazardOngoing