Device recall
Z-0868-2010: IDEAL MAXPAC TOTAL SYSTEM (USA), Sterile and Nonpyrogenic, ETO or Gamma…
FDA device recall · Class III · Medtronic Inc
Key facts
| Recall number (Z-number) | Z-0868-2010 |
|---|---|
| Recall event | 54237 |
| Product | IDEAL MAXPAC TOTAL SYSTEM (USA) , Sterile and Nonpyrogenic, ETO or Gamma Sterilized, Medtronic Perfusion Systems, Model TS9453R29, TS9453R30, TS1470R1, TS1442R1, TS9800R32, TS8299R4. |
| Product code | KRI |
| Recalling firm | Medtronic Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Apr 20, 2011 |
| 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