Device recall
Z-1019-2007: Various Sizes of Sterile Polyglycolic Acid Synthetic Surgical Suture-NDR…
FDA device recall · Class II · Teleflex Creek Dr
Key facts
| Recall number (Z-number) | Z-1019-2007 |
|---|---|
| Recall event | 38220 |
| Product | Various Sizes of Sterile Polyglycolic Acid Synthetic Surgical Suture-NDR, POLYGLY 2-0 C-2/CST43 2N36, Catalog #833-135 |
| Product code | GAM |
| Recalling firm | Teleflex Creek Dr |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 14, 2008 |
| 510(k) numbers | K992088 |
| 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