Recall Z-0959-05 ยท IQZ Hand, External Limb Component, Powered
Motion Control, Inc.
Spectre brand AC wall adapter to be used with ProControl 2 or ProHand battery powered upper limb prosthesis.
| Date | Jul 6, 2005 (initiated Feb 1, 2005) |
| Status | Terminated |
| Reason | Incorrect AC wall adapter was distributed with prostheses. Incorrect use of adapters could damage the battery and cause a potential fire hazard. |
| Root cause | Other |
| Action | Consignees were notified by phone and letter on 2/3/2005. |
| Quantity | 20 units |
| Distribution | CA, DC, FL, NJ, OH, PA, SC, TN, TX, and Puerto Rico. No military, government or foreign distribution. |
| FDA record | Open on fda.gov |
510(k) clearances named in this recall
This recall record lists no 510(k) number.