Device recall
Z-1552-2009: Medtronic Ideal MAXPAC Total System, Catalog Numbers: TS1262R6, TS1262R7…
FDA device recall · Class II · Medtronic Cardiovascular Revascularization & Surgical Therap
Key facts
| Recall number (Z-number) | Z-1552-2009 |
|---|---|
| Recall event | 51785 |
| Product | Medtronic Ideal MAXPAC Total System, Catalog Numbers: TS1262R6, TS1262R7, TS1420R, TS1420R1, TS1442R, TS1446R, TS1464T, TS1470R, TS1470T1, TS1480R3, TS1480R5, TS1480R6, TS1487R, TS1487R2, TS8040R28, TS8108R6, TS8163R10, TS8387R5, TS9412R3, TS9453R28, TS9764R9, TS9800R28, TS9800R29, TS9800R31… |
| Product code | OEU |
| Recalling firm | Medtronic Cardiovascular Revascularization & Surgical Therap |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 22, 2012 |
| FEI number | 1000116158 |
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