Atlas FDA

Permobil Chairman 2K powered wheelchair, Model 1280

FDA device recall Z-0671-03 · posted 2003-03-21 · Terminated

Recall details

Recalling firm
Permobile Inc.
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.
Action taken
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
Status
Terminated
Product code
I--TI
Quantity affected
1582
Distribution
Nationwide, Puerto Rico, Canada
Date initiated
2003-01-01
Date posted
2003-03-21
Date terminated
2008-06-25
Location
Lebanon, TN

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Related 510(k) clearances

RecordFirmDate
PERMOBIL POWERED WHEELCHAIR 1280 (K991658)Permobil AB1999-10-08