Device recall
Z-0643-05: Manual Mechanical Wheelchair, 16'' seat,, maximum patient weight: 250 lbs…
FDA device recall · Class II · Cypress Medical Products, Ltd.
Key facts
| Recall number (Z-number) | Z-0643-05 |
|---|---|
| Recall event | 31147 |
| Product | Manual Mechanical Wheelchair, 16'' seat, , maximum patient weight: 250 lbs.; Marketed by McKesson Corporation, McKesson Medical-Surgical, Richmond, VA 23228, Made in China; the wheelchairs were sold in the following configurations: reorder 16-7910: Fixed Full Arm, Swing Footrest reorder 16-7911… |
| Product code | IOR |
| Recalling firm | Cypress Medical Products, Ltd. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 19, 2005 |
| 510(k) numbers | K002670, K002671 |
| FEI number | 1451040 |
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