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 28481–28500 of 29,201 recalls
Recalled Item: Sarns Modular Perfusion System 8000 base Recalled by Terumo Cardiovascular...
The Issue: Terumo Cardiovascular Systems has received several reports of malfunctions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom surgical kits and trays: GEO-MED TOTAL KNEE PACK PGYBK Recalled by...
The Issue: Surgical kits and trays contain Stryker Hytrel Togas which were recalled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Equinoxe Anatomic Replicator Plate Intended for Primary and Reverse Total...
The Issue: Exactech, Inc. initiated a recall of Equinoxe Replicator Plates, Equinoxe...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Equinoxe Reverse Glenosphere Locking Screw Intended for Primary and Reverse...
The Issue: Exactech, Inc. initiated a recall of Equinoxe Replicator Plates, Equinoxe...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Equinoxe Fixed Angle Replicator Plate Intended for Primary and Reverse...
The Issue: Exactech, Inc. initiated a recall of Equinoxe Replicator Plates, Equinoxe...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Octane-C Cervical Recalled by Exactech, Inc. Due to Exactech, Inc. initiated...
The Issue: Exactech, Inc. initiated a recall of Equinoxe Replicator Plates, Equinoxe...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AngioDynamics Angiographic catheter --- Soft-Vu (JB-1) Non-braided. ---...
The Issue: AngioDynamics is recalling one lot of Soft-Vu Angiographic catheters because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STA Satellite Automated Multi-Parameter Analyzer This system is a fully...
The Issue: Following a single customer complaint that incorrect INR values were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hitachi Echelon MRI System/Oasis MRI Recalled by Hitachi Medical Systems...
The Issue: Hitachi discovered a software error with a feature called Multi-Planar...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Equinoxe Reverse Shoulder Fracture Adapter Tray Screw Intended for Primary...
The Issue: Exactech, Inc. initiated a recall of Equinoxe Replicator Plates, Equinoxe...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Equinoxe Reverse Compression Screw Intended for Primary and Reverse Total...
The Issue: Exactech, Inc. initiated a recall of Equinoxe Replicator Plates, Equinoxe...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Pump Module Model 8100 (formerly Medley Pump Module) Subsequent...
The Issue: The recall was initiated because Carefusion has identified a potential risk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity PACS IW by GE Healthcare Dynamic Imaging Solutions is Recalled by...
The Issue: Multiple issues were identified with the GE Centricity PACS-IW system that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The 2.7mm Drilling Guide is a reusable instrument used in Recalled by...
The Issue: Integra' s quality system noted an adverse trend in complaints for breakage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Xcelera Connect Recalled by Philips Healthcare Inc. Due to Xcelera...
The Issue: Xcelera Connect R2.1 L 1 SP2 , incomplete information arriving from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: seprafilm¿ Procedure Pack ADHESION BARRIER Re-order Number: 5086-02 Product...
The Issue: Sterility of product may be compromised due to packaging defect
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE has become aware of...
The Issue: GE has become aware of multiple issues affecting the Dash 3000/4000/5000 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: seprafilm¿ Single Site ADHESION BARRIER Re-order Number: 6641-01 Product...
The Issue: Sterility of product may be compromised due to packaging defect
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE has become aware of...
The Issue: GE has become aware of multiple issues affecting the Dash 3000/4000/5000...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carestream DRX-1 System Battery --- Made in U.S.A. for Carestream Health...
The Issue: Carestream DRX-1 System batteries manufactured before June 2012 due to two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.