Device recall
Z-2286-2010: Deknatel Bondek Plus Polyglycolic Absorbable Surgical Sutures, Bon+BG BR 3-0 DSL…
FDA device recall · Class II · Telefelx Medical
Key facts
| Recall number (Z-number) | Z-2286-2010 |
|---|---|
| Recall event | 54474 |
| Product | Deknatel Bondek Plus Polyglycolic Absorbable Surgical Sutures, Bon+BG BR 3-0 DSL 19 1N (45cm), Teleflex Medical. Bondek and Bondek Plus Synthetic Absorbable Surgical Sutures intended uses are in general surgical procedures where general soft tissue approximation and/or ligation are performed… |
| Product code | GAM |
| Recalling firm | Telefelx Medical |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 19, 2011 |
| 510(k) numbers | K905482 |
| FEI number | 3005747797 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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