Device recall
Z-0991-2019: AVE 2 Birthing Bed
FDA device recall · Class II · Linet Spol. S.r.o.
Key facts
| Recall number (Z-number) | Z-0991-2019 |
|---|---|
| Recall event | 81927 |
| Product | AVE 2 Birthing Bed |
| Product code | HDD |
| Recalling firm | Linet Spol. S.r.o. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 31, 2023 |
| FEI number | 3008058231 |
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