Device recall
Z-1015-2007: Various Types, Sterile/Nonsterile Stainless Steel Nonabsorable Surgical…
FDA device recall · Class II · Teleflex Creek Dr
Key facts
| Recall number (Z-number) | Z-1015-2007 |
|---|---|
| Recall event | 38220 |
| Product | Various Types, Sterile/Nonsterile Stainless Steel Nonabsorable Surgical Sutures-SS Wire, STL MF 7 HSCX48 1N 18 X2, Catalog #29-6567M2; SS Wire, STL MF 6 HSCX48 1N 18 X6, Catalog #29-6619M6, SS Wire, STL MF 6 K-60 1N 18"X8, Catalog #29-7270M8,SS Wire, STL MF 5 K-60/ B-60 1N18 X7, Catalog #29-9001M7… |
| Product code | GAM |
| Recalling firm | Teleflex Creek Dr |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 14, 2008 |
| 510(k) numbers | K930740 |
| 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