Device recall
Z-2781-2020: AVE 2 Birthing Bed - Product Usage: is designated to be used by mothers ready…
FDA device recall · Class III · Linet Americas
Key facts
| Recall number (Z-number) | Z-2781-2020 |
|---|---|
| Recall event | 85094 |
| Product | AVE 2 Birthing Bed - Product Usage: is designated to be used by mothers ready for spontaneous vaginal delivery and also as aid to search for individual positions providing relief in all delivery stages including postpartum period. Birthing bed is not intended for use as a general hospital bed. |
| Product code | HDD |
| Recalling firm | Linet Americas |
| Recall class | Class III |
| Status | Open, Classified |
| FEI number | 3008007426 |
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