Device recall
Z-2748-2020: Pleur-Evac Adult-Ped Wet, LF Intl Eng, product code: A-8000I - Product Usage…
FDA device recall · Class II · TELEFLEX MEDICAL INC
Key facts
| Recall number (Z-number) | Z-2748-2020 |
|---|---|
| Recall event | 85952 |
| Product | Pleur-Evac Adult-Ped Wet, LF Intl Eng, product code: A-8000I - Product Usage: CHEST DRAINAGE: To evacuate air and/or fluid from the chest cavity or mediastinum. To help prevent air and/or fluid from re-accumulating in the chest cavity or mediastinum. To help re-establish and maintain normal… |
| Product code | KDQ |
| Recalling firm | TELEFLEX MEDICAL INC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 2, 2026 |
| FEI number | 3005747797 |
At a glance
- None 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