Device recall
Z-1254-06: VIASYS Healthcare Disposable Bar Electrodes. Re-order No. 019-435600. Single Use…
FDA device recall · Class III · Nicolet Biomedical Div of Viasys Healthcare
Key facts
| Recall number (Z-number) | Z-1254-06 |
|---|---|
| Recall event | 35416 |
| Product | VIASYS Healthcare Disposable Bar Electrodes. Re-order No. 019-435600. Single Use only. Manufactured in the U.S.A. for VIASYS Healthcare, 5225 Verona Road, Bldg 2, Madison, WI USA 53711-4495..Each box contains 10 pouches of Bar Electrodes and each pouch contains 10 electrodes |
| Product code | GXZ |
| Recalling firm | Nicolet Biomedical Div of Viasys Healthcare |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Dec 27, 2006 |
| 510(k) numbers | K010019 |
| 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