Device recall
Z-1107-04: LIFEPAK 12 defibrillator/monitor Part Numbers: VLP12-02-000000 through…
FDA device recall · Class II · Medtronic Physio Control Corp
Key facts
| Recall number (Z-number) | Z-1107-04 |
|---|---|
| Recall event | 29025 |
| Product | LIFEPAK 12 defibrillator/monitor Part Numbers: VLP12-02-000000 through VLP12-02-005003, AVLP12-02-000000 through AVLP12-02-005003, DVLP12-02-000000 through DVLP12-02-005003, EVLP12-02-000000 through EVLP12-02-005003, FVLP12-02-000000 through FVLP12-02-005003, LVLP12-02-000000 through… |
| Product code | MKJ |
| Recalling firm | Medtronic Physio Control Corp |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 6, 2006 |
| 510(k) numbers | K012274 |
| FEI number | 3015876 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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