Device recall
Z-0039-2018: Pilling Knife Handles: a) REF 352950 b) REF 352953 c) REF 352951 d) REF 352957…
FDA device recall · Class II · Teleflex Medical
Key facts
| Recall number (Z-number) | Z-0039-2018 |
|---|---|
| Recall event | 78207 |
| Product | Pilling Knife Handles: a) REF 352950 b) REF 352953 c) REF 352951 d) REF 352957 e) REF 352952 : Reusable surgical knife handles, which are intended for use with blades which are inserted into a slot in the handle. |
| Product code | GDZ |
| Recalling firm | Teleflex Medical |
| Recall class | Class II |
| Status | Completed |
| 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