Device recall
Z-2972-2018: DORO LUCENT Transitional Member, REF 1101.026 Component of headrest system used…
FDA device recall · Class I · Pro-Med Instruments Gmbh
Key facts
| Recall number (Z-number) | Z-2972-2018 |
|---|---|
| Recall event | 80628 |
| Product | DORO LUCENT Transitional Member, REF 1101.026 Component of headrest system used in open and percutaneous craniotomies and spinal surgeries |
| Product code | HBL |
| Recalling firm | Pro-Med Instruments Gmbh |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Nov 19, 2020 |
| 510(k) numbers | K032331 |
| FEI number | 3003923584 |
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