FDA Device recall Z-2467-2018
T2100 Micro flex Drive Treadmill, powered Product Usage: Powered exercise equipment consist of powered devices intended for medical purpose…
- FDA Device
- Class II
- terminated
- Published 2018-07-25
On 2018-07-25 the FDA classified a Class II recall of T2100 Micro flex Drive Treadmill, powered Product Usage: Powered exercise equipment consist of powered devices intended for medical purpose… by Ge Medical Systems Ultrasound And Primary Care Diagnostics Ll, citing 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 i….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2467-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-04-02 |
| Published | 2018-07-25 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Ge Medical Systems Ultrasound And Primary Care Diagnostics Ll |
| Distribution | US |
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
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.
Identifiers
| code_info | Treadmill Model Numbers 2026182-004, 2026182-002. Known lot/serial numbers: SBC07152197SA, SBC07372859SA, SJV14412914…Treadmill Model Numbers 2026182-004, 2026182-002. Known lot/serial numbers: SBC07152197SA, SBC07372859SA, SJV14412914SA, SBC12038975SA, SBC12169265SA, SJV14052101SA, SJV14092190SA, SBC10376789SA, SBC12079098SA, SBC12079100SA, 5460609, 5448740, SBC12049021SA, SBC12059040SA, SBC12139235SA, SBC07112098SA, SBC07132153SA, SBC10226425SA, SBC12129213SA, SBC06331301SA, SBC10336719SA, SBC06261147SA, SBC09485858SA, SBC10376798SA, SBC12069076SA, SBC12119201SA, SBC12149236SA, SBC11298412SA, SBC11308452SA, SBC11308470SA, SBC12038973SA, SBC12099151SA, SBC12119205SA, SBC12129227SA, SJV14212408SA, SBC06180862SA, SJV14382840SA, SJV14372765SA, SBC11148122SA, SBC11288388SA, SBC12089134SA, SBC06040465SA, SBC12049001SA, SBC12049015SA, SBC12049022SA, SBC12049025SA, SBC11418622SA, SBC11418624SA, SBC11418633SA, SJV12380433SA, SBC06170848SA, SBC06170856SA, SBC06170857SA, SBC05490198SA, SBC08514915SA, SJV12430536SA, SJV14412927SA, SBC06030436SA, SBC06040441SA, SBC06210965SA, 8588656, SBC05510384SA, SBC0613072 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2467-2018%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.