Device recall
Z-0529-2007: Skytron Infinity Series surgical light, 5 bulbs in 1 - 22' diameter lighthead…
FDA device recall · Class II · Skytron, Div. The KMW Group, Inc
Key facts
| Recall number (Z-number) | Z-0529-2007 |
|---|---|
| Recall event | 37120 |
| Product | Skytron Infinity Series surgical light, 5 bulbs in 1 - 22' diameter lighthead, Manufactured by Dai-ichi Shomei Co., Ltd., Made in Japan; Models IF22, IF22B, IF22LH, IF22LHH-B, IF22M-S, IN22, IN22EL, IN22LH and IF22(EL). |
| Product code | FTD |
| Recalling firm | Skytron, Div. The KMW Group, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 18, 2009 |
| 510(k) numbers | K915285 |
| FEI number | 1825014 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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