Drug recall
GE Healthcare, Treadmill T2100 and Treadmill T2000 with power cord part numbers 408930-001 Rev E, 408930-002…
FDA recall event 70535 · Class II · GE Healthcare
Key facts
| Event ID | 70535 |
|---|---|
| Recall numbers | Z-1285-2015 |
| Recalling firm | GE Healthcare |
| Product type | Devices |
| Products | GE Healthcare, Treadmill T2100 and Treadmill T2000 with power cord part numbers 408930-001 Rev E, 408930-002 Rev C, or 2028038-008 Rev B. Also Field Replaceable Unit P/N s 408930-001 Rev E, 408930-002… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Potential safety issue due to improper assembly associated with the power cords of T2100 and T2000 Treadmills. |
| Initiation date | Feb 16, 2015 |
| Report date | Mar 25, 2015 |
| Termination date | Jun 23, 2017 |
| City | Waukesha |
| State | WI |
| Country | United States |
| FEI number | 2126677 |
At a glance
- 1–9 Products in this recall
- 10–99 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: