Device recall
Z-1142-2021: Covidien Parietex hydrophilic anatomical mesh 15 cm x 10 cm polyester left…
FDA device recall · Class II · Covidien Llc
Key facts
| Recall number (Z-number) | Z-1142-2021 |
|---|---|
| Recall event | 87179 |
| 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 |
| Product code | FTL |
| Recalling firm | Covidien Llc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 14, 2023 |
| 510(k) numbers | K173796 |
| FEI number | 1282497 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database