Drug recall
Covidien Parietex hydrophilic anatomical mesh 15 cm x 10 cm polyester left - Product Usage: designed for the…
FDA recall event 87179 · Class II · Covidien Llc
Key facts
| Event ID | 87179 |
|---|---|
| Recall numbers | Z-1142-2021 |
| Recalling firm | Covidien Llc |
| Product type | Devices |
| Products | 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… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| 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… |
| Initiation date | Jan 13, 2021 |
| Report date | Mar 3, 2021 |
| Termination date | Feb 14, 2023 |
| City | Mansfield |
| State | MA |
| Country | United States |
| FEI number | 1282497 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: