TRACHEAL INTUBATION FIBERSCOPE OLYMPUS LF-GP, Model Number: LF-GP
Reported: December 20, 2023 Initiated: September 28, 2023 #Z-0557-2024
Product Description
TRACHEAL INTUBATION FIBERSCOPE OLYMPUS LF-GP, Model Number: LF-GP
Reason for Recall
Fiberscopes do not have adequate data to support that the suction flow rate meets the device specification.
Details
- Recalling Firm
- Olympus Corporation of the Americas
- Units Affected
- 75
- Distribution
- Worldwide - US Nationwide distribution in the states of AK, AL, AZ, CA, GA, IL, IN, MA, MD, MI, NC, NJ, OH, TX, UT, VA, WA, WV & AP (Armed Forces Pacific) and the countries of OUS: EMEA, Japan and Australia.
- Location
- Center Valley, PA
Frequently Asked Questions
What product was recalled? ▼
TRACHEAL INTUBATION FIBERSCOPE OLYMPUS LF-GP, Model Number: LF-GP. Recalled by Olympus Corporation of the Americas. Units affected: 75.
Why was this product recalled? ▼
Fiberscopes do not have adequate data to support that the suction flow rate meets the device specification.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on December 20, 2023. Severity: Moderate. Recall number: Z-0557-2024.
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