Device recall
Z-1334-04: 8870 software application card versions AAA 02, BBB 04, BBC 02, and BBD 01…
FDA device recall · Class I · Medtronic Inc, Neurological & Spinal Division
Key facts
| Recall number (Z-number) | Z-1334-04 |
|---|---|
| Recall event | 29849 |
| Product | 8870 software application card versions AAA 02, BBB 04, BBC 02, and BBD 01, which is used in conjunction with the Model 8840 N''Vision Clinician Programmer. |
| Product code | LKK |
| Recalling firm | Medtronic Inc, Neurological & Spinal Division |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Dec 13, 2005 |
| PMA numbers | P860004 |
| FEI number | 2182207 |
At a glance
- None 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