Olympus Corporation of the Americas Recall 92779
Description: Olympus Tracheal Intubation Fiberscope, Models LF-P & LF-V.
Olympus Corporation of the Americas Recall 92779 Information
| Status | Ongoing |
| Mandated? | Voluntary: Firm initiated |
| Recall Number | Z-2501-2023 |
| Event ID | 92779 |
| Event Description | Olympus Tracheal Intubation Fiberscope, Models LF-P & LF-V. |
| Product Type | Devices |
| Distribution | US Nationwide distribution. |
| Quantity | 2127 units |
| Recall Reason | Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large. |
| Device Classification | 20230906 |
| Device Code Info | UDI-DI: 04953170051098, 04953170452932, & 04953170156250; All Serial Numbers. |
| Center Classification Date | 20230831 |
| Recall Initiation Date | 20230727 |
| Recalling Firm | Olympus Corporation of the Americas |
| Initial Notification | Letter |
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