Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
T2100 Micro flex Drive Treadmill Recalled by GE Medical Systems Ultrasound & Primary Care Diagnostics, LL Due to A performance issue with customer owned spare parts,...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact GE Medical Systems Ultrasound & Primary Care Diagnostics, LL directly.
Affected Products
T2100 Micro flex Drive Treadmill, powered Product Usage: Powered exercise equipment consist of powered devices intended for medical purposes, such as to redevelop muscles or restore motion to joints or for use as an adjunct treatment for obesity. Specifically the T210 Treadmill is intended for use in Exercise Testing, facilitating accurate blood pressure measurements and exercise testing within speed range of 0-13.5 miles per hour.
Quantity: 3,721 devices total
Why Was This Recalled?
A performance issue with customer owned spare parts, T2100 Microflex drive (2026182-002 or 2026182-004), was not addressed with a previous safety correction. If these parts were installed from customer owned stock on the T2100 Treadmill, uncontrolled walking belt motion during a stress exercise test could occur.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About GE Medical Systems Ultrasound & Primary Care Diagnostics, LL
GE Medical Systems Ultrasound & Primary Care Diagnostics, LL has 12 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report