# FDA recall Z-1142-2021

> **Covidien Llc** · Class II · device recall initiated 2021-01-13.

## Product

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

## 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.

## Key facts

- **Recall number:** Z-1142-2021
- **Recalling firm:** Covidien Llc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2021-01-13
- **Report date:** 2021-03-03
- **Termination date:** 2023-02-14

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Mansfield, MA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1142-2021

## Citation

> AI Analytics. FDA recall Z-1142-2021. Retrieved 2026-09-09 from https://api.ai-analytics.org/recall/Z-1142-2021. Source: US FDA. Licensed CC0.

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