Device recall
Z-1472-2026: Adapt Pump, Model/Catalog Number: 61600200-Adapt Pump, component of Adapt…
FDA device recall · Class II · Agiliti Health - Ellis
Key facts
| Recall number (Z-number) | Z-1472-2026 |
|---|---|
| Recall event | 98332 |
| Product | Adapt Pump, Model/Catalog Number: 61600200-Adapt Pump, component of Adapt support surfaces (Adapt Air, Adapt Air EX, Adapt Air Pro, Adapt Air Pro EX, Adapt Convertible, Adapt Convertible EX), sofware version 1.3.0; Mattress, Air Flotation, Alternating Pressure |
| Product code | FNM |
| Recalling firm | Agiliti Health - Ellis |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3002693132 |
At a glance
- None 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