Device recall
Z-1014-2007: Various Sizes of Sterile Polygycolic Acid Synthetic Surgical Sutures -Bondek…
FDA device recall · Class II · Teleflex Creek Dr
Key facts
| Recall number (Z-number) | Z-1014-2007 |
|---|---|
| Recall event | 38220 |
| Product | Various Sizes of Sterile Polygycolic Acid Synthetic Surgical Sutures -Bondek, BON+ BG BR 1 HRX27 1N70CM, Catalog # EP1082N, Bondek, BON+ BG BR 2-0 HR26+ 1RN4X45CM, Catalog # EP8027XN, Bondek, BON+ BG BR 0 12X45CM, Catalog # EP8656N, Bondek, BON+ BG BR 2 12X45CM, Catalog # EP8658N |
| 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