Device recall
Z-0054-2013: TORQ Sternal Closure Device. The common name is TWISTER, WIRE. The model number…
FDA device recall · Class II · Kardium
Key facts
| Recall number (Z-number) | Z-0054-2013 |
|---|---|
| Recall event | 63111 |
| Product | TORQ Sternal Closure Device. The common name is TWISTER, WIRE. The model number is TQ01A. The Catalog numbers are: 17-00001: TORQ Sternal Closure Device Shipping Carton (6-10 packs), Sterile and, 15-00001 (or 17-00002): TORQ Sternal Closure Device 10-pack - Sterile. The device is supplied… |
| Product code | HXS |
| Recalling firm | Kardium |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 5, 2013 |
| FEI number | 3009214225 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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