Device recall
Z-0063-2007: AC-powered Adjustable Hospital Bed. (ICCG Bed) Affected Model numbers…
FDA device recall · Class III · Invacare Corporation
Key facts
| Recall number (Z-number) | Z-0063-2007 |
|---|---|
| Recall event | 36410 |
| Product | AC-powered Adjustable Hospital Bed. (ICCG Bed) Affected Model numbers: IH820-3MDLX, IHSC900DLX, IH820-3MDLX-QS, IH820-3MPDLX-QS, SC900-80WDLX-QSP, SC900-80PDLX-QSP, IH820-3MDLX-AE-333PS, SC90080GDLX-AE-366PA, SC90080GDLX-AE-333PS, IH820-3MDLX-AE-366PS, IH820-3MDLX-AE-333PA, IH820-3MDLX-AE-366PA and… |
| Product code | LLI |
| Recalling firm | Invacare Corporation |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Oct 5, 2009 |
| FEI number | 1031452 |
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