RegWardenFDA facility compliance records
Recall

Class II — Battle Creek Equipment Co.

Recalling firmBattle Creek Equipment
Registered facilityBattle Creek Equipment (the firm's only registered facility)
ClassificationClass II
StatusTerminated
ReasonProducts manufactured with the SPT cord have a known failure mode of sparking,causing smoke, fire and burns.
ProductModel 055: Thermophore Classic, Professional Quality, Deep-Heat Therapy, Model 055 Large 14' x 27", Model 056: Thermophore Classic, Professional Quality Deep-Heat Therapy, Model 056 Medium 14" x 14", Model 077: Thermophore Classic Professional Quality Deep-Heat Therapy, Model 077 Petite 4"x 17",Model 095: Thermophore Classic, Professional Quality Deep-Heat Therapy, Model 095 Large 14" x 27 Model 096: Thermophore Classic, Professional Quality Deep-Heat therapy Model 096, Medium, 14" x 14" Model 097: Thermophore Classic, Professional quality Deep-Heat Therapy, Model 097 , Petite, 4" …
Quantity99,060
DistributionDistributed within the United States, Canada, Mexico, Puerto Rico and Columbia
Initiated2016-09-15
Classified2016-11-03
Terminated2018-01-11
Recall numberZ-0349-2017
InitiationVoluntary: Firm initiated

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)

Cite this record

RegWarden. “Class II recall — Battle Creek Equipment Co. (Z-0349-2017).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/73286/

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