Device recall
Z-0839-05: Dunlee DA 200 PRO & MX 200 PRO CT X-Ray Tube Housing Assembly (989600088401)…
FDA device recall · Class II · Dunlee
Key facts
| Recall number (Z-number) | Z-0839-05 |
|---|---|
| Recall event | 31457 |
| Product | Dunlee DA 200 PRO & MX 200 PRO CT X-Ray Tube Housing Assembly (989600088401); replacement x-ray tube housing assemblies; Dunlee, 555 North Commerce Street, Aurora, Illinois 60504 U.S.A.; part number 875-01 |
| Product code | ITY |
| Recalling firm | Dunlee |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 20, 2005 |
| FEI number | 1483239 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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