Device recall
Z-1225-2009: Medtronic Mosaic Porcine Bioprostheses with Cinch, Heart Valve; Model 305…
FDA device recall · Class III · Medtronic Inc
Key facts
| Recall number (Z-number) | Z-1225-2009 |
|---|---|
| Recall event | 51220 |
| Product | Medtronic Mosaic Porcine Bioprostheses with Cinch, Heart Valve; Model 305; Catalog #s 305C21AA, 305C2701, 305C2301, 305C2501, and 305C2901; Sterile LC; Rx only; Medtronic Inc 710 Medtronic Parkway, Minneapolis, MN 55432-5604, Manufactured at: Santa Ana, Ca. Indicated for the replacement of… |
| Product code | DYE |
| Recalling firm | Medtronic Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | May 22, 2012 |
| PMA numbers | P990064 |
| 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