Device recall
Z-1225-2007: BMSI "MicroJack" PN 672-510000 patient interface electrode connection device…
FDA device recall · Class II · Nicolet Biomedical Div of Viasys Healthcare
Key facts
| Recall number (Z-number) | Z-1225-2007 |
|---|---|
| Recall event | 38424 |
| Product | BMSI "MicroJack" PN 672-510000 patient interface electrode connection device used during electroencephalography (EEG) /Epilepsy Monitoring evaluations with various EEG monitoring systems. The MicroJack is used with BMSI Models 2000, 3000, 4000, 5000 & 6000, and is used with the BMSI kit upgraded… |
| Product code | GWQ |
| Recalling firm | Nicolet Biomedical Div of Viasys Healthcare |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 10, 2011 |
| 510(k) numbers | K891405 |
| FEI number | 3010611950 |
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