FDA Medical Device Recalls (openFDA)
Motion Control, Inc.: Spectre brand AC wall adapter to be used with ProControl 2 or ProHand battery powered upper limb prosthesis.
- Recall number
- Z-0959-05
- Recalling firm
- Motion Control, Inc.
- Product
- Spectre brand AC wall adapter to be used with ProControl 2 or ProHand battery powered upper limb prosthesis.
- Status
- Terminated
- Initiated
- 2005-02-01
- Posted
- 2005-07-06
- Terminated
- 2008-10-07
- 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.
- Lot, serial or model codes
- Part number PD1880 PL6A
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- IQZ
- Firm FEI
- 3001237006
- Firm city
- Salt Lake City
- Firm state
- UT
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28