Drug recall
Colonovideoscope Model CF-H180AL
FDA recall event 90218 · Class II · Olympus Corporation of the Americas
Key facts
| Event ID | 90218 |
|---|---|
| Recall numbers | Z-1274-2022 |
| Recalling firm | Olympus Corporation of the Americas |
| Product type | Devices |
| Products | Colonovideoscope Model CF-H180AL |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | A (Camera unit) CCD intended for a different model of colonoscope may have been installed in the CF-H180AL, viewing angle would be narrower than a normal CF-H180AL and the use of EndoTherapy devices… |
| Initiation date | Apr 22, 2022 |
| Report date | Jun 29, 2022 |
| Termination date | Mar 13, 2024 |
| 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: