Covidien Parietex hydrophilic anatomical mesh 15 cm x 10 cm polyester… — Class II medical device recall Z-1142-2021
Terminated recall by Covidien Llc, reported 2021-03-03, distributed nationwide. incorrect device is contained in the package. The packaging label indicates that the device is for left side u
| Recall number | Z-1142-2021 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Covidien Llc, Mansfield, MA, United States |
| Recall initiated | 2021-01-13 |
| Classified | 2021-02-22 |
| Reported by FDA | 2021-03-03 |
| Terminated | 2023-02-14 |
| Distributed | Nationwide (US) |
| Countries outside the US | DE, ES, FR, GB, LU |
| Quantity | 129 units |
| Reason classes | labeling |
| Lot numbers | SUH0709M |
| Model numbers | TECT1510AL |
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
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1142-2021. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.