T2100 Micro flex Drive Treadmill — Class II medical device recall Z-2467-2018
Terminated recall by GE Medical Systems Ultrasound & Primary Care Diagnostics, LL, reported 2018-07-25, distributed nationwide. A performance issue with customer owned spare parts, T2100 Microflex drive (2026182-002 or 2026182-004), was n
| Recall number | Z-2467-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | GE Medical Systems Ultrasound & Primary Care Diagnostics, LL, Milwaukee, WI, United States |
| Recall initiated | 2018-04-02 |
| Classified | 2018-07-16 |
| Reported by FDA | 2018-07-25 |
| Terminated | 2024-04-30 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, AR, AT, AU, BD, BE, BG, BH, BO, BR, CA, CH, CL, CN, CO, CR, CY, CZ, DE, DO, DZ, EC, EE, EG, ES, GR, HK, HR, ID, IE, IL, IN, IQ, IT, JM, JO, KE, KR, KW, KY, LB, LK, MA, MX, NG, NP, NZ, PA, PE, PH, PK, PL, PY, QA, RO, RS, RU, SG, SI, SK, SV, TH, TN, TR, TT, TW, UA, UY, VE, VN, ZA |
| Quantity | 3,721 devices |
| Serial numbers | 310080281, 49004822, 5448740, 5460609, 80147358, 8588656, 8607326, 8684256, 8831712, 9039955, 9081830, JV14092187SA, SBC05440028SA, SBC05440033SA, SBC05450040SA, SBC05450042SA, SBC05450051SA, SBC05450052SA, SBC05450053SA, SBC05450073SA, SBC05460079SA, SBC05460098SA, SBC05460100SA, SBC05460104SA, SBC05460107SA and 475 more |
| Model numbers | 2026182-002, 2026182-004 |
Product
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.
Reason for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2467-2018. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.