Z-1400-06

Pronto M51 Wheelchair, component- seat

Name: Z-1400-06 Pronto M51 Wheelchair, component- seat
Creator: Invacare Corporation
Published: 2006-06-14
License: https://open.fda.gov/license/

Invacare GmbH / initiated 2006-06-14 / Terminated

FDA source

Invacare Corporation began a recall of Pronto M51 Wheelchair, component- seat on 2006-06-14. The reason FDA records is "Some of the wheelchairs were distributed with seats that did not have a seat positioning strap". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-1400-06
Status: Terminated
Initiated: 2006-06-14
Posted: 2006-08-10
Terminated: 2007-08-22
Recalling firm: Invacare GmbH
Product: Pronto M51 Wheelchair, component- seat
Product code: ITI Wheelchair, Powered
Reason for recall: Some of the wheelchairs were distributed with seats that did not have a seat positioning strap.
FDA root cause: Other
Action: The recalling firm sent a recall letter, dated 06/06 to consignees.
Quantity in commerce: 853 units
Distribution: Nationwide.
Product codes and lots: There is no code on the individual seat. Recall covers seats on wheelchairs distributed between 03/14/2006 and 04/07/2006.

Product code ITI

K021680Class IIInvacare Powered Wheelchairs, Models M50, M51, M71 & M91Invacare Corp. / cleared 2002-06-18

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)