Device recall
Z-1295-2014: Sutures, Non-absorbable, Steel, Monofilament and Multifilament, Sterile, Rx…
FDA device recall · Class II · Teleflex Medical
Key facts
| Recall number (Z-number) | Z-1295-2014 |
|---|---|
| Recall event | 67733 |
| Product | Sutures, Non-absorbable, Steel, Monofilament and Multifilament, Sterile, Rx only, Product Usage: A smooth or threaded metallic bone fixation fastener is a device intended to be implanted that consists of a stiff wire segment or rod made of alloys, such as cobalt-chromium-molybdenum and stainless… |
| Product code | GAT |
| Recalling firm | Teleflex Medical |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 15, 2017 |
| 510(k) numbers | K021019 |
| 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