Device recall
Z-1560-2014: Deknatel Teleflex Medical Stainless Steel 2 (metric 5) Monofilament Stainless…
FDA device recall · Class II · Teleflex Medical
Key facts
| Recall number (Z-number) | Z-1560-2014 |
|---|---|
| Recall event | 67711 |
| Product | Deknatel Teleflex Medical Stainless Steel 2 (metric 5) Monofilament Stainless Steel Suture, Nonabsorbable Surgical Suture, U.S.P. Used for fixation of bone fractures, for bone reconstructions, as a guide pin for insertion of other implants, or it may be implanted through the skin so that a pulling… |
| Product code | GAQ |
| Recalling firm | Teleflex Medical |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 14, 2017 |
| 510(k) numbers | K930738 |
| FEI number | 3005747797 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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