Battle Creek Equipment Co.
FDA adverse event reports naming Battle Creek Equipment Co. as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: BATTLE CREEK EQUIPMENT CO..
- Total reports
- 1,233
- Deaths
- 1
- Injuries
- 8
- Malfunctions
- 1,217
Reports per year
Source: FDA adverse event reports by year received, 2000–2017. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
Recent recalls
- TerminatedDevice Design
Model 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" x 17", Model 255: Thermophore Classic Plus, Professional Quality Deep-Heat Therapy, Model 255 Large,14" x 27", Model 256: Thermophore Classic Plus Professional Quality Deep-Heat Therapy, Model 256, Medium, 14" X 14 Model 277: Thermophore Classic Plus Professional Quality Deep-Heat Therapy, Model 277, Petite , 4" x 17" Used for the temporary relief of joint and muscle pain.
Products manufactured with the SPT cord have a known failure mode of sparking,causing smoke, fire and burns.
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