Z-0622-2007

HoMedics Thera P Standard size Dry Heating Pad; Model No. HP-100 (UPC 031262003621)

Name: Z-0622-2007 HoMedics Thera P Standard size Dry Heating Pad; Model No. HP-100 (UPC 031262003621)
Creator: HoMedics, Inc.
Published: 2007-02-09
License: https://open.fda.gov/license/

FKA Distributing Co., LLC / initiated 2007-02-09 / Terminated

FDA source

HoMedics, Inc. began a recall of HoMedics Thera P Standard size Dry Heating Pad; Model No. HP-100 (UPC 031262003621) on 2007-02-09. The reason FDA records is "Heating pads may have a loose electrical connection, which could result in excessive heat being generated that poses a risk of patient burns, fire, and property damage". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0622-2007
Status: Terminated
Initiated: 2007-02-09
Posted: 2007-03-21
Terminated: 2010-01-04
Recalling firm: FKA Distributing Co., LLC
Product: HoMedics Thera P Standard size Dry Heating Pad; Model No. HP-100 (UPC 031262003621).
Product code: IRT Pad, Heating, Powered
Reason for recall: Heating pads may have a loose electrical connection, which could result in excessive heat being generated that poses a risk of patient burns, fire, and property damage.
FDA root cause: Other
Action: Press release issued on 2/9/07 instructing consumers to return the product to store of purchase or Homedics. Retail stores notified via recall letter issued on 2/9/07. Retail stores are being instructed to accept returns and to post placards to notify customers of the recall.
Quantity in commerce: 292,108 of all models
Distribution: Nationwide and Canada.
Product codes and lots: All units with a four digit date code ending in ''01'' (this code is located on the hand control and on the bottom panel of the heat pad box).

Product code IRT

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)