Z-1697-2009

Foot Choice Therapeutic Foot Massager, Model Number YS-322. The device is a heated foot massager intended for...

Name: Z-1697-2009 Foot Choice Therapeutic Foot Massager, Model Number YS-322. The device is a heated foot massager intended for...
Creator: Suarez Corporation Industries
Published: 2006-08-07
License: https://open.fda.gov/license/

Suarez Corporation Industries / initiated 2006-08-07 / Terminated / root cause: design

FDA source

Suarez Corporation Industries began a recall of Foot Choice Therapeutic Foot Massager, Model Number YS-322. The device is a heated foot massager intended for over the counter use on 2006-08-07. The reason FDA records is "Complaints of product causing burns to consumers". As of 2026-09-10, the recall status on record is Terminated, and MDM tags the root cause as design.

Recall record

Recall number: Z-1697-2009
Status: Terminated
Initiated: 2006-08-07
Posted: 2009-08-07
Terminated: 2010-10-13
Recalling firm: Suarez Corporation Industries
Product: Foot Choice Therapeutic Foot Massager, Model Number YS-322. The device is a heated foot massager intended for over the counter use.
Product code: ILY Lamp, Infrared, Therapeutic Heating
Reason for recall: Complaints of product causing burns to consumers.
Root cause tag: design
FDA root cause: Device Design
Action: On August 9- August 14, 2006, the firm sent a letter to all customers which included an "Important Customer Reminder." The Reminder now listed additional warnings about serious burns occurring regardless of the control settings. Direct questions to Suarez Corporation Industries by calling 1-330-494-5504.
Quantity in commerce: 71,512 units
Distribution: Nationwide and Canada.
Product codes and lots: No Lot Code (All massagers manufactured and shipped between 11/04/2005 - 06/29/2006).

Product code ILY

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)