Device recall
Z-1990-2009: BHM Combi Sling, 100% Polyester Shell/100% Polyester Strap; soft polyester net…
FDA device recall · Class II · B.H.M. Medical, Inc.
Key facts
| Recall number (Z-number) | Z-1990-2009 |
|---|---|
| Recall event | 51999 |
| Product | BHM Combi Sling, 100% Polyester Shell/100% Polyester Strap; soft polyester net fabric sling for ceiling and floor patient lifts; BHM, Magog, Canada, made in China. Part 626002: Combi Deluxe - Medium, capacity 68-113 kg, 150-250 lbs; Part 626002M: Combi Mesh Deluxe - Medium, capacity 68-113 kg… |
| Product code | FNG |
| Recalling firm | B.H.M. Medical, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 7, 2011 |
| FEI number | 3002655016 |
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