Drug recall
EVIS EXERA III Colonovideoscope-For endoscopy and endoscopic surgery within the lower digestive tract…
FDA recall event 91411 · Class II · Olympus Corporation of the Americas
Key facts
| Event ID | 91411 |
|---|---|
| Recall numbers | Z-1132-2023 |
| Recalling firm | Olympus Corporation of the Americas |
| Product type | Devices |
| Products | EVIS EXERA III Colonovideoscope-For endoscopy and endoscopic surgery within the lower digestive tract (including the anus, rectum, sigmoid colon, colon, and ileocecal valve) Model/Serial: CF-Q180AL |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | A single CF-Q180AL colonovideoscope was utilized in a veterinary endoscopy procedure in advance of being assigned to a medical facility as a service loaner in error, potential for microbial… |
| Initiation date | Dec 21, 2022 |
| Report date | Feb 22, 2023 |
| 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: