Device recall
Z-2675-2014: The synthetic non-absorbable surgical sutures CARDIOXYL are composed of a…
FDA device recall · Class II · Peters Surgical
Key facts
| Recall number (Z-number) | Z-2675-2014 |
|---|---|
| Recall event | 68721 |
| Product | The synthetic non-absorbable surgical sutures CARDIOXYL are composed of a polyester [poly(ethylene terephtalate)] braids, with or without PLEDGET of different sizes. CARDIOXYL braids are coated with polysiloxane. CARDIOXYL sutures are green dyed (D&C green # 6, CI 61565) and white (undyed). Some… |
| Product code | GAT |
| Recalling firm | Peters Surgical |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 13, 2017 |
| 510(k) numbers | K060163 |
| FEI number | 3004060107 |
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