Device recall
Z-2676-2014: The synthetic non-absorbable surgical sutures CARDIOFLON Evolution are composed…
FDA device recall · Class II · Peters Surgical
Key facts
| Recall number (Z-number) | Z-2676-2014 |
|---|---|
| Recall event | 68721 |
| Product | The synthetic non-absorbable surgical sutures CARDIOFLON Evolution are composed of polyester [poly(ethylene terephtalate)] braids, coated, with or without PLEDGETS of different sizes. CARDIOFLON Evolution sutures are green dyed (D&C green # 6, CI 61565) and white (undyed). Some packs are composed of… |
| 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