Device recall
Z-1173-2009: Medtronic STREAMLINE Bipolar Temporary Myocardial Pacing Lead, 6495, Sterile EO…
FDA device recall · Class III · Medtronic Inc
Key facts
| Recall number (Z-number) | Z-1173-2009 |
|---|---|
| Recall event | 51292 |
| Product | Medtronic STREAMLINE Bipolar Temporary Myocardial Pacing Lead, 6495, Sterile EO, REF 6495F, Medtronic, INC., Minneapolis, MN 55432 |
| Product code | LDF |
| Recalling firm | Medtronic Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | May 7, 2011 |
| 510(k) numbers | K963898 |
| FEI number | 3001504994 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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