Device recall
Z-0888-2017: Medi Choice Arm Slings ASL 2103 Small 7.5 x 12.5 Inch 1/EA, 24 ENCA ASL 2104…
FDA device recall · Class II · Owens & Minor Distribution, Inc.
Key facts
| Recall number (Z-number) | Z-0888-2017 |
|---|---|
| Recall event | 75649 |
| Product | Medi Choice Arm Slings ASL 2103 Small 7.5 x 12.5 Inch 1/EA, 24 ENCA ASL 2104 Medium 8 x 15 Inch 1/EA, 24 ENCA ASL 2105 Large 8.5 x 17.5 Inch 1/EA, 24 ENCA ASL 2106 Extra-Large 9 x 20 Inch 1/EA, 24 ENCA ASL 2150 Universal 7 x 18 Inch 1/EA, 24 ENCA Medical - An arm sling is a device intended for… |
| Product code | ILI |
| Recalling firm | Owens & Minor Distribution, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 9, 2018 |
| FEI number | 3003753847 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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