Device recall
Z-1270-2020: Teleflex Medical Disposable Aortic Punch, in the following sizes: a) 2.8 mm, REF…
FDA device recall · Class II · TELEFLEX MEDICAL INC
Key facts
| Recall number (Z-number) | Z-1270-2020 |
|---|---|
| Recall event | 84722 |
| Product | Teleflex Medical Disposable Aortic Punch, in the following sizes: a) 2.8 mm, REF DP-28K b) 3.6 mm, REF DP-36K c) 4.0 mm, REF DP-40K d) 4.4 mm, REF DP-44K e) 4.8 mm, REF DP-48K f) 5.2 mm, REF DP-52K g) 5.6 mm, REF DP-56K h) 6.0 mm, REF DP-60K i) 2.8 mm, REF MDP-28K j) 3.6 mm, REF MDP-36K k) 4.0 mm… |
| Product code | DWS |
| Recalling firm | TELEFLEX MEDICAL INC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 24, 2021 |
| 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