Device recall
Z-1645-2010: Ceiling Suspensions (Surgical Light and Flat Panel Suspensions); Catalog…
FDA device recall · Class II · Stryker Communications Corp
Key facts
| Recall number (Z-number) | Z-1645-2010 |
|---|---|
| Recall event | 55477 |
| Product | Ceiling Suspensions (Surgical Light and Flat Panel Suspensions); Catalog Numbers: 0682000863, 06820001009, 0682001010, 0682001076, 0682000864, 0682000857, 0682000858, 0682001077, 0682000865, 0682001011, 0682001078, 0682000866, 0682001012, 0682001080, 0682000867, 0682000959, 0682001079, 0682000850… |
| Product code | BRY |
| Recalling firm | Stryker Communications Corp |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 24, 2011 |
| 510(k) numbers | K031068, K033132 |
| FEI number | 3002975342 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 Products in the same recall event
- 100–999 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