Device recall
Z-2156-2021: Affinity Four Birthing Bed-used as a birthing bed for women of child bearing age…
FDA device recall · Class II · Hill-Rom, Inc.
Key facts
| Recall number (Z-number) | Z-2156-2021 |
|---|---|
| Recall event | 88185 |
| Product | Affinity Four Birthing Bed-used as a birthing bed for women of child bearing age in an LDR (Labor, Delivery, Recovery) or LDRP (Labor, Delivery, Recovery, Postpartum) setting within the acute care Labor and Delivery market Model Numbers: P3700B, P3700C, P3700D, & P3700E |
| Product code | KNC |
| Recalling firm | Hill-Rom, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 6, 2024 |
| 510(k) numbers | K915779 |
| FEI number | 1824206 |
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