Covidien Llc: Medical Device Recall in 2021 - (Recall #: Z-1142-2021)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2021.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: January 13, 2021

Date Posted: March 3, 2021

Recall Number: Z-1142-2021

Event ID: 87179

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

Status: Terminated

Product Quantity: 129 units WW

Code Information:

Lot Number: SUH0709M

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated