Drug recall
HF Cable WA00014A, Endoscopic electrosurgical unit and accessories
FDA recall event 75601 · Class II · Olympus Corporation of the Americas
Key facts
| Event ID | 75601 |
|---|---|
| Recall numbers | Z-0754-2017 |
| Recalling firm | Olympus Corporation of the Americas |
| Product type | Devices |
| Products | HF Cable WA00014A, Endoscopic electrosurgical unit and accessories |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Software malfunction that results in incorrect generation or display of error codes. |
| Initiation date | Nov 3, 2016 |
| Report date | Dec 21, 2016 |
| Termination date | Feb 6, 2019 |
| City | Center Valley |
| State | PA |
| Country | United States |
| FEI number | 2429304 |
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: