Drug recall
Lokomat Pro, Catalog Numbers 30003 LokomatPro L6.2 120V AD; 30004 LokomatPro L6.2 120V Kombi; 30005…
FDA recall event 85857 · Class II · Hocoma AG
Key facts
| Event ID | 85857 |
|---|---|
| Recall numbers | Z-2418-2020 |
| Recalling firm | Hocoma AG |
| Product type | Devices |
| Products | Lokomat Pro, Catalog Numbers 30003 LokomatPro L6.2 120V AD ; 30004 LokomatPro L6.2 120V Kombi; 30005 LokomatPro L6.2 120V PE; 30683 LokomatPro L6.2 110V FD PE; 30684 LokomatPro L6.2 110V FD Kombi… |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The motor controller may fail, which can potentially lead to an error in functionality of the Body Weights Support Rope, which means that the rope can go up or down in an uncontrolled way. |
| Initiation date | Jun 8, 2020 |
| Report date | Jul 1, 2020 |
| City | Volketswil |
| Country | Switzerland |
| FEI number | 3003781275 |
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: