Device recall
Z-1582-2016: Pleur-evac Chest Drainage System, Dry Suction/Dry Seal Control, REF A-6000-08LF…
FDA device recall · Class II · Teleflex Medical
Key facts
| Recall number (Z-number) | Z-1582-2016 |
|---|---|
| Recall event | 73676 |
| Product | Pleur-evac Chest Drainage System, Dry Suction/Dry Seal Control, REF A-6000-08LF, Rx Only, Teleflex Medical. Product Usage: Pleur-Evacs are sterile, single-use, chest drainage systems intended for post-operative use |
| Product code | CAC |
| Recalling firm | Teleflex Medical |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 30, 2025 |
| 510(k) numbers | K140205 |
| FEI number | 3005747797 |
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