Recall Z-0349-2017— Battle Creek Equipment Co.

Class II FDA medical device recall by Battle Creek Equipment Co., initiated 2016-09-15, terminated 2018-01-11. FDA's recall record names no specific 510(k) clearance for this event. Product: 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.. Reason: Products manufactured with the SPT cord have a known failure mode of sparking,causing smoke, fire and burns..

Recalling firm

Battle Creek Equipment Co.

Classification

Class II

Status

Terminated

Initiated

2016-09-15

Terminated

2018-01-11

Firm location

Fremont, IN, United States

Data sourced from openFDA. This site is unofficial and independent of the FDA.