Z-0959-05

Spectre brand AC wall adapter to be used with ProControl 2 or ProHand battery powered upper limb prosthesis

Name: Z-0959-05 Spectre brand AC wall adapter to be used with ProControl 2 or ProHand battery powered upper limb prosthesis
Creator: Motion Control, Inc.
Published: 2005-02-01
License: https://open.fda.gov/license/

Motion Control, Inc. / initiated 2005-02-01 / Terminated

FDA source

Motion Control, Inc. began a recall of Spectre brand AC wall adapter to be used with ProControl 2 or ProHand battery powered upper limb prosthesis on 2005-02-01. The reason FDA records is "Incorrect AC wall adapter was distributed with prostheses. Incorrect use of adapters could damage the battery and cause a potential fire hazard". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0959-05
Status: Terminated
Initiated: 2005-02-01
Posted: 2005-07-06
Terminated: 2008-10-07
Recalling firm: Motion Control, Inc.
Product: Spectre brand AC wall adapter to be used with ProControl 2 or ProHand battery powered upper limb prosthesis.
Product code: IQZ Hand, External Limb Component, Powered
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.
FDA root cause: Other
Action: Consignees were notified by phone and letter on 2/3/2005.
Quantity in commerce: 20 units
Distribution: CA, DC, FL, NJ, OH, PA, SC, TN, TX, and Puerto Rico. No military, government or foreign distribution.
Product codes and lots: Part number PD1880 PL6A

Product code IQZ

The FDA recall record names no cleared device, and no clearance has been matched to it.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)