Device recall
Z-0058-04: FLEXICAIR II, Low Airloss Therapy unit.This unit is similar to MC3 but does not…
FDA device recall · Class II · Hill-Rom Manufacturing, Inc.
Key facts
| Recall number (Z-number) | Z-0058-04 |
|---|---|
| Recall event | 27202 |
| Product | FLEXICAIR II, Low Airloss Therapy unit.This unit is similar to MC3 but does not have the utility shelf above the foodboard, patient scale or alternate CPR function actuators. |
| Product code | IOQ |
| Recalling firm | Hill-Rom Manufacturing, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 1, 2004 |
| 510(k) numbers | K863047 |
| FEI number | 1045510 |
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