Drug recall
T2100 Micro flex Drive Treadmill, powered Product Usage: Powered exercise equipment consist of powered devices…
FDA recall event 80165 · Class II · GE Medical Systems Ultrasound & Primary Care Diagnostics, LL
Key facts
| Event ID | 80165 |
|---|---|
| Recall numbers | Z-2467-2018 |
| Recalling firm | GE Medical Systems Ultrasound & Primary Care Diagnostics, LL |
| Product type | Devices |
| 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… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| 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… |
| Initiation date | Apr 2, 2018 |
| Report date | Jul 25, 2018 |
| Termination date | Apr 30, 2024 |
| City | Milwaukee |
| State | WI |
| Country | United States |
| FEI number | 3005860720 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: