Spectre brand AC wall adapter to be used with ProControl 2 or ProHand battery powered upper limb prosthesis.
FDA Recall Z-0959-05 · Posted 2005-07-06
Recalling FirmMotion Control, Inc.
Recall StatusTerminated
Product CodeIQZ
Date Initiated2005-02-01
Date Terminated2008-10-07
Product Quantity20 units
Reason for Recall
Incorrect AC wall adapter was distributed with prostheses. Incorrect use of adapters could damage the battery and cause a potential fire hazard.
Firm Action
Consignees were notified by phone and letter on 2/3/2005.
Root Cause
Other
Distribution Pattern
CA, DC, FL, NJ, OH, PA, SC, TN, TX, and Puerto Rico. No military, government or foreign distribution.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.