Olympus Corporation of the Americas: Medical Device Recall in 2023 - (Recall #: Z-0557-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

TRACHEAL INTUBATION FIBERSCOPE OLYMPUS LF-GP, Model Number: LF-GP

Product Classification:

Class II

Date Initiated: September 28, 2023

Date Posted: December 20, 2023

Recall Number: Z-0557-2024

Event ID: 93433

Reason for Recall:

Fiberscopes do not have adequate data to support that the suction flow rate meets the device specification.

Status: Ongoing

Product Quantity: 75

Code Information:

UDI-DI: 04953170340215 & UDI-DI: 04953170061998. Serial numbers: 2515143, 2515181, 2515449, 2515549, 2615760, 2615761, 2615763, 2615825, 2615830, 2615831, 2616057, 2616130, 2616199, 2716417, 2817430, 2917855, 2917867, 2917997, 2918003, 2918010, 2918012, 2918030, 2018337, 2018435, 2018486, 2018543, 2018571, 2018675, 2319768, 2319820, 2510582, 2621001.

Distribution Pattern:

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.

Voluntary or Mandated:

Voluntary: Firm initiated