Drug recall
Colonoscope, Model Number CF-H180AL.
FDA recall event 93832 · Class II · Olympus Corporation of the Americas
Key facts
| Event ID | 93832 |
|---|---|
| Recall numbers | Z-1205-2024, Z-1206-2024, Z-1207-2024, Z-1208-2024, Z-1209-2024, Z-1210-2024, Z-1211-2024, Z-1212-2024, Z-1213-2024, Z-1214-2024 |
| Recalling firm | Olympus Corporation of the Americas |
| Product type | Devices |
| Products | Colonoscope, Model Number CF-H180AL., Colonoscope, Model Number CF-HQ190I., Colonoscope, Model Number CF-HQ190L., Colonoscope, Model Number CF-Q180AL., Colonoscope, Model Number PCF-H180AL. and 5 more |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Specific repaired colonovideoscopes were assembled without an adhesive which protects them from certain physical conditions such as high levels of vibration, fluctuation in temperature or severe shock… |
| Initiation date | Jan 11, 2024 |
| Report date | Mar 6, 2024 |
| City | Center Valley |
| State | PA |
| Country | United States |
| FEI number | 2429304 |
At a glance
- 10–99 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: