Z-1421-06

Guardian 5 inch Walker Wheel Kits, Model Numbers: 07722-8, 07722G, 07722-5, 07722-8B, 07725. Made in China by...

Name: Z-1421-06 Guardian 5 inch Walker Wheel Kits, Model Numbers: 07722-8, 07722G, 07722-5, 07722-8B, 07725. Made in China by...
Creator: A & E Industries, Ltd.
Published: 2006-06-30
License: https://open.fda.gov/license/

Zhongshan A&e Machinery Industry Co., Ltd / initiated 2006-06-30 / Terminated

FDA source

A & E Industries, Ltd. began a recall of Guardian 5 inch Walker Wheel Kits, Model Numbers: 07722-8, 07722G, 07722-5, 07722-8B, 07725. Made in China by A&E Machinery Industry Co., Ltd on 2006-06-30. The reason FDA records is "Walker wheel hubs may fracture, causing walker to collapse to one side". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-1421-06
Status: Terminated
Initiated: 2006-06-30
Posted: 2006-08-24
Terminated: 2011-07-20
Recalling firm: Zhongshan A&e Machinery Industry Co., Ltd
Product: Guardian 5 inch Walker Wheel Kits, Model Numbers: 07722-8, 07722G, 07722-5, 07722-8B, 07725. Made in China by A&E Machinery Industry Co., Ltd.
Product code: ITJ Walker, Mechanical
Reason for recall: Walker wheel hubs may fracture, causing walker to collapse to one side.
FDA root cause: Other
Action: Consignees were notified by letter on 06/30/2006.
Quantity in commerce: 63,153 units.
Distribution: Worldwide distribution --- USA and countries of Bangladesh, Chile, Japan, and Mexico
Product codes and lots: Model numbers 07722-8, 07722G, 07722-5, 07722-8B, 07725. Lot numbers 0603, 0604, 0605.

Product code ITJ

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)