Device recall
Z-1226-2009: Hancock II Bioprostheses with Cinch, Heart Valve, Model # T505 & T510; Catalog…
FDA device recall · Class III · Medtronic Inc
Key facts
| Recall number (Z-number) | Z-1226-2009 |
|---|---|
| Recall event | 51220 |
| Product | Hancock II Bioprostheses with Cinch, Heart Valve, Model # T505 & T510; Catalog #s T505C2501, T505C2101, T505U25ID , T505C2301, T505C2301, T505C2501, T505C2101, T510C29ID, T510C25ID, and T510C27ID; Sterile LC; Rx only; Medtronic Inc 710 Medtronic Parkway, Minneapolis, MN 55432-5604, Manufactured at… |
| Product code | DYE |
| Recalling firm | Medtronic Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | May 22, 2012 |
| PMA numbers | P980043 |
| FEI number | 3001504994 |
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