Device recall
Z-1153-2009: ALM Prismatic Surgical Light 9551 DF; Maquet SA. ALM PRISMATIC (PRC) Surgical…
FDA device recall · Class II · MAQUET Inc.
Key facts
| Recall number (Z-number) | Z-1153-2009 |
|---|---|
| Recall event | 51297 |
| Product | ALM Prismatic Surgical Light 9551 DF; Maquet SA. ALM PRISMATIC (PRC) Surgical Lights are used to provide visible illumination for the surgical field or for the examination of the patient. PRC is designed to eliminate shadow, reduce reflected heat, and illuminate surgical incisions of all depths… |
| Product code | FTD |
| Recalling firm | MAQUET Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 29, 2009 |
| 510(k) numbers | K882613 |
| FEI number | 3008355164 |
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