FDAClass IIJuly 12, 2023

Trackmaster recall

TRACKMASTER, TREADMILL GE T2100-ST2 220V CHINA, MODEL NUMBER 317-07927GE CHINA

Why was Trackmaster recalled?

Treadmill malfunction: drive PCB can misread the signals and stop or reverse and then accelerate forward.

What should I do if I have this product?

The recall is ongoing. Follow the firm and FDA instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

UDI/DI 00860176000675, Serial Numbers: GEDC-6765, GEDC-6766, GEDC-6767, GEDC-6768, GEDC-6849, GEDC-6850, GEDC-6851, GEDC-6852, GEDC-6995, GEDC-6996, GEDC-6997, GEDC-6998, GEDC-6999, GEDC-7000, GEDC-7001, GEDC-7002, GEDC-7003, GEDC-7004, GEDC-7005, GEDC-7006, GEDC-7007, GEDC-7008, GEDC-7009, GEDC-7010, GEDC-7011, GEDC-7375, GEDC-7376, GEDC-7377, GEDC-7378, GEDC-7379, GEDC-7380, GEDC-7466, GEDC-7467, GEDC-7468, GEDC-7469, GEDC-7470, GEDC-7471, GEDC-7472, GEDC-7473, GEDC-7474, GEDC-7475, GEDC-7476, GEDC-7477, GEDC-7478, GEDC-7479, GEDC-7480, GEDC-7481, GEDC-7482, GEDC-7888, GEDC-7889, GEDC-7890, GEDC-7892, GEDC-7894, GEDC-7896, GEDC-7897, GEDC-7901, GEDC-7902, GEDC-7906, GEDC-7907, GEDC-7908, GEDC-7913, GEDC-7914, GEDC-7915, GEDC-7916, GEDC-7917, GEDC-7918, GEDC-7919, GEDC-7920, GEDC-7921, GEDC-7922, GEDC-7923, GEDC-7924, GEDC-7925, GEDC-7926, GEDC-7927, GEDC-7928, GEDC-7929, GEDC-7930, GEDC-7931, GEDC-7932, GEDC-7933, GEDC-7934, GEDC-7935, GEDC-7936, GEDC-7937, GEDC-7939, GEDC-7940, GEDC-7941, GEDC-7949, GEDC-7952, GEDC-7953, GEDC-7954, GEDC-7955, GEDC-7956, GEDC-8018

Product
TRACKMASTER, TREADMILL GE T2100-ST2 220V CHINA, MODEL NUMBER 317-07927GE CHINA
Recalling firm
Full Vision Inc
Quantity
95 units
Distribution
USA (Nationwide), Australia, Bahrain, Canada, Chile, Colombia, Costa Rica, Dominican Republic, FINLAND, Guatemala, HONG KONG, India, Indonesia, Israel, Mexico, NEW ZEALAND, Nicaragua, Panama, PARAQUAY, Peru, Philippines, Saudi Arabia, Singapore, SOUTH KOREA, Thailand, Ukraine, United Arab Emirates, United Kingdom, Uruguay
Recall date
July 12, 2023
Classification
Class II
Status
Ongoing
Agency
FDA (device)
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