RecallDepth

Covidien Parietex hydrophilic anatomical mesh 15 cm x 10 cm polyester left - Product Usage: designed for the repair of inguinal hernias via laparoscopic or posterior open procedures Item Code: TECT1510AL

Company
Covidien Llc
Recall Initiated
January 13, 2021
Terminated
February 14, 2023
Recall Number
Z-1142-2021
Quantity
129 units WW
Firm Location
Mansfield, MA

Reason for Recall

incorrect device is contained in the package. The packaging label indicates that the device is for left side use, the product inside the package is for right side use. Use of an opposite side mesh can result in implant failure and hernia recurrence

Distribution

Worldwide distribution - US Nationwide distribution in the state of MA and the countries of France, French Guiana, Germany, Luxembourg, Spain, United Kingdom.

Lot / Code Info

Lot Number: SUH0709M

Root Cause

Under Investigation by firm

Action Taken

Medtronic issued Urgent Medical Device Recall letter via Federal Express and/or certified mail beginning January 13, 2021. The letter states reason for recall, health risk and action to take:: " Immediately quarantine and discontinue use of the affected item codes and lots. " Return affected product. " Forward the information to anyone who they have distributed affected Covidien Parietex" Hydrophilic Anatomical Mesh. " Complete the Recalled Product Return Form. Inventory within Medtronic control and customer returned products will be scrapped. Questions regarding this communication, please contact your Medtronic representative or Customer Service at 800-962-9888, option 2.

More recalls by Covidien Llc

View all recalls by this company →