Device recall
Z-0526-04: Stryker brand Firstcare Ultra Maternity bed and Stryker brand Adel Maternity…
FDA device recall · Class II · Stryker Medical
Key facts
| Recall number (Z-number) | Z-0526-04 |
|---|---|
| Recall event | 28135 |
| Product | Stryker brand Firstcare Ultra Maternity bed and Stryker brand Adel Maternity bed, 220 volt, model 5012, with night light. |
| Product code | HDD |
| Recalling firm | Stryker Medical |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 7, 2004 |
| 510(k) numbers | K950889 |
| FEI number | 1831750 |
At a glance
- 1–9 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