Device recall
Z-0808-2007: Product is an EO Sterile, Blue Polypropylene monofilament synthetic…
FDA device recall · Class II · C P Medical
Key facts
| Recall number (Z-number) | Z-0808-2007 |
|---|---|
| Recall event | 37756 |
| Product | Product is an EO Sterile, Blue Polypropylene monofilament synthetic nonabsorbable surgical suture with needle, size 3/0 (2.0 Metric), NFS-2, 19 mm Needle. Product is wrapped in a five-fold card with inserted flap ends (overwrap). A label is placed on the overwrap and the packet is then inserted into… |
| Product code | GAW |
| Recalling firm | C P Medical |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 1, 2008 |
| 510(k) numbers | K001185 |
| FEI number | 3002609049 |
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