Olympus Tracheal Intubation Fiberscope, Models LF-DP, LF-GP, & LF-TP.
Reported: September 6, 2023 Initiated: July 27, 2023 #Z-2504-2023
Product Description
Olympus Tracheal Intubation Fiberscope, Models LF-DP, LF-GP, & LF-TP.
Reason for Recall
Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large.
Details
- Recalling Firm
- Olympus Corporation of the Americas
- Units Affected
- 10801 units
- Distribution
- US Nationwide distribution.
- Location
- Center Valley, PA
Frequently Asked Questions
What product was recalled? ▼
Olympus Tracheal Intubation Fiberscope, Models LF-DP, LF-GP, & LF-TP.. Recalled by Olympus Corporation of the Americas. Units affected: 10801 units.
Why was this product recalled? ▼
Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on September 6, 2023. Severity: Moderate. Recall number: Z-2504-2023.
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