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. 2,609 recalls have been distributed to Louisiana in the last 12 months.

51,202 total recalls
2,609 in last 12 months

Showing 1676116780 of 51,202 recalls

Medical DeviceJanuary 19, 2021· ReNovo, Inc.

Recalled Item: Various reprocessed products: PROVISION Recalled by ReNovo, Inc. Due to...

The Issue: Non-sterile product was shipped to customers labelled as sterile.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 19, 2021· Merit Medical Systems, Inc.

Recalled Item: Heartspan Transseptal Needles Recalled by Merit Medical Systems, Inc. Due to...

The Issue: The labeled needle tip curvature of specific lots of transseptal needles may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 19, 2021· Sky Medical Supplies and Equipments LLC

Recalled Item: AntIbody to SARS-CoV-2 - Product Usage: (Colloidal Gold) for IgG/IgM...

The Issue: Distributed COVID test kits without emergency use authorization.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 19, 2021· Boston Scientific Corporation

Recalled Item: Captivator II Single-Use Polypectomy Snares Outer box UPN Recalled by Boston...

The Issue: Packaging Incomplete Seal. Users noted an incomplete pouch seal prior to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 19, 2021· Stryker Sustainability Solutions

Recalled Item: Stryker Sustainability Solutions Ethicon Endo-Surgery Recalled by Stryker...

The Issue: Product was distributed without receiving regulatory clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 18, 2021· Smiths Medical ASD Inc.

Recalled Item: Tube Tracheostomy and Tube Cuff Recalled by Smiths Medical ASD Inc. Due to...

The Issue: Smiths Medical became aware that three lot numbers of a specific model of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2021· RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

Recalled Item: CervAlign Anterior Cervical Plate System-Cervalign Recalled by RTI Surgical,...

The Issue: Locking mechanism has been observed to disassociate either intraoperatively...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2021· RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

Recalled Item: CervAlign Anterior Cervical Plate System-Cervalign Recalled by RTI Surgical,...

The Issue: Locking mechanism has been observed to disassociate either intraoperatively...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2021· RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

Recalled Item: CervAlign Anterior Cervical Plate System-Cervalign Recalled by RTI Surgical,...

The Issue: Locking mechanism has been observed to disassociate either intraoperatively...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2021· RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

Recalled Item: CervAlign Anterior Cervical Plate System-Cervalign Recalled by RTI Surgical,...

The Issue: Locking mechanism has been observed to disassociate either intraoperatively...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2021· RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

Recalled Item: CervAlign Anterior Cervical Plate System-Cervalign Recalled by RTI Surgical,...

The Issue: Locking mechanism has been observed to disassociate either intraoperatively...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2021· Medtronic Vascular

Recalled Item: Medtronic 6F Launcher Guide Catheter 100 cm EBU 3.0 Model Number: LA6EBU30...

The Issue: Sterility may be compromised due to an unsealed pouch

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2021· Northgate Technologies, Inc.

Recalled Item: ConMed 50L abdominal insufflator Recalled by Northgate Technologies, Inc....

The Issue: An internal tubing component in the flow path was made with incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2021· Northgate Technologies, Inc.

Recalled Item: Steris CO2MPACT Endoscopic Insufflator system Recalled by Northgate...

The Issue: An internal tubing component in the flow path was made with incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2021· RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

Recalled Item: CervAlign Anterior Cervical Plate System-Cervalign Recalled by RTI Surgical,...

The Issue: Locking mechanism has been observed to disassociate either intraoperatively...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2021· RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

Recalled Item: CervAlign Anterior Cervical Plate System-Cervalign Recalled by RTI Surgical,...

The Issue: Locking mechanism has been observed to disassociate either intraoperatively...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2021· Biomet, Inc.

Recalled Item: Central Screw 6.5x25mm - Product Usage: used as a sterile Recalled by...

The Issue: Zimmer Biomet is conducting a lot specific medical device recall for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2021· RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

Recalled Item: CervAlign Anterior Cervical Plate System-Cervalign Recalled by RTI Surgical,...

The Issue: Locking mechanism has been observed to disassociate either intraoperatively...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2021· RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

Recalled Item: CervAlign Anterior Cervical Plate System-Cervalign Recalled by RTI Surgical,...

The Issue: Locking mechanism has been observed to disassociate either intraoperatively...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2021· RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

Recalled Item: CervAlign Anterior Cervical Plate System-Cervalign Recalled by RTI Surgical,...

The Issue: Locking mechanism has been observed to disassociate either intraoperatively...

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

Class II — Potential Health HazardOngoing