Z-0039-2007

Eagle Parts and Products Model 624EZ Power Wheel Chairs with internally threaded wheel mount motors

Name: Z-0039-2007 Eagle Parts and Products Model 624EZ Power Wheel Chairs with internally threaded wheel mount motors
Creator: Eagle Parts and Products
Published: 2006-07-11
License: https://open.fda.gov/license/

Eagle Parts & Products, Inc. / initiated 2006-07-11 / Terminated

FDA source

Eagle Parts and Products began a recall of Eagle Parts and Products Model 624EZ Power Wheel Chairs with internally threaded wheel mount motors on 2006-07-11. The reason FDA records is "The wheel hub bolts may loosen resulting in the wheels coming off". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0039-2007
Status: Terminated
Initiated: 2006-07-11
Posted: 2006-10-19
Terminated: 2012-09-05
Recalling firm: Eagle Parts & Products, Inc.
Product: Eagle Parts and Products Model 624EZ Power Wheel Chairs with internally threaded wheel mount motors.
Product code: ITI Wheelchair, Powered
Reason for recall: The wheel hub bolts may loosen resulting in the wheels coming off.
FDA root cause: Other
Action: Consignees were first notified by letter on 07/11/2006. Recall was expanded to include all units on 07/28/2006.
Quantity in commerce: 365 units (total for both models)
Distribution: AL, FL, GA, KY, NC, SC TN, TX
Product codes and lots: Serial numbers 624EZ0010 through 624EZ0513.

Product code ITI

K990122Class IIIndependence 624Eagle Parts & Products, Inc. / cleared 1999-06-25

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)