Device recall
Z-1708-2014: Monoswift PGCL [poly (glycolide-co-caprolactone)] Absorbable Surgical Suture…
FDA device recall · Class II · C P Medical Inc.
Key facts
| Recall number (Z-number) | Z-1708-2014 |
|---|---|
| Recall event | 68153 |
| Product | Monoswift PGCL [poly (glycolide-co-caprolactone)] Absorbable Surgical Suture; USP size 3/0 PGCL; part number L936. Product is labeled sterile. The product is sealed inside an inner foil pouch with an outside Tyvek pouch. It is an undyed, monofilament synthetic absorbable suture with needle, size 3/0… |
| Product code | NEW |
| Recalling firm | C P Medical Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 12, 2014 |
| 510(k) numbers | K030786 |
| 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