Device recall
Z-1955-2012: CIVCO General Purpose Sensor, Non-sterile reusable general purpose…
FDA device recall · Class II · Civco Medical Instruments Inc
Key facts
| Recall number (Z-number) | Z-1955-2012 |
|---|---|
| Recall event | 61793 |
| Product | CIVCO General Purpose Sensor, Non-sterile reusable general purpose electromagnetic sensor, for use with 3D Guidance medSAFE trackers, Ref. 610-1067. The firm name on the label is CIVCO, Kalona, IA. The kit contains sensor component part number 410-240. The general purpose sensor within the kit is… |
| Product code | IYO |
| Recalling firm | Civco Medical Instruments Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 7, 2015 |
| 510(k) numbers | K092619 |
| FEI number | 1937223 |
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