FDA Device recall Z-2504-2023
Olympus Tracheal Intubation Fiberscope, Models LF-DP, LF-GP, & LF-TP
- FDA Device
- Class II
- ongoing
- Published 2023-09-06
On 2023-09-06 the FDA classified a Class II recall of Olympus Tracheal Intubation Fiberscope, Models LF-DP, LF-GP, & LF-TP by Olympus, citing complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2504-2023 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-07-27 |
| Published | 2023-09-06 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Olympus |
| Distribution | US |
Product
Olympus Tracheal Intubation Fiberscope, Models LF-DP, LF-GP, & LF-TP.
Reason
Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large.
Identifiers
| code_info | UDI-DI: 04953170136856, 04953170340192, 04953170061998, 04953170340215, 04953170317576, & 04953170136825; All Serial Numbers. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2504-2023%22
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