Motion Control, Inc. Spectre brand AC wall adapter to be used with ProControl 2 or ProHand battery powered upper limb prosthesis. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Spectre brand AC wall adapter to be used with ProControl 2 or ProHand battery powered upper limb prosthesis.
Brand
Motion Control, Inc.
Lot Codes / Batch Numbers
Part number PD1880 PL6A
Products Sold
Part number PD1880 PL6A
Motion Control, Inc. is recalling Spectre brand AC wall adapter to be used with ProControl 2 or ProHand battery powered upper limb pro due to Incorrect AC wall adapter was distributed with prostheses. Incorrect use of adapters could damage the battery and cause a potential fire hazard.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Incorrect AC wall adapter was distributed with prostheses. Incorrect use of adapters could damage the battery and cause a potential fire hazard.
Recommended Action
Per FDA guidance
Consignees were notified by phone and letter on 2/3/2005.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
CA, FL, NJ, OH, OR, PA, SC, TN, TX, DC, PR
Page updated: Jan 10, 2026