Permobil Chairman 2K powered wheelchair, Model 1280
FDA Recall Z-0671-03 · Posted 2003-03-21
Recalling FirmPermobile Inc.
Recall StatusTerminated
Product CodeI--TI
Date Initiated2003-01-01
Date Terminated2008-06-25
Product Quantity1582
Reason for Recall
Incidents were reported where a drive wheel has come off its motor axle, due either to loosening of the wheel bolt or a broken wheel bolt.
Firm Action
Permobil Inc has notified its field representatives of the voluntary recall and these representatives have been provided with lists of each Chairman 2K serial number and the Dealer to which the wheelchair was sold.
Root Cause
Other
Distribution Pattern
Nationwide, Puerto Rico, Canada
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.