Olympus Corporation of the Americas: Medical Device Recall in 2023 - (Recall #: Z-2490-2023)

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:

Olympus Bronchovideoscope, Models BF-1T150, BF-1T60, BF-MP60, BF-P150, BF-P60, BF-PE2, BF-TE2, BF-XT160.

Product Classification:

Class II

Date Initiated: July 27, 2023

Date Posted: September 6, 2023

Recall Number: Z-2490-2023

Event ID: 92779

Reason for Recall:

Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large.

Status: Ongoing

Product Quantity: 1715 units

Code Information:

UDI-DI: 04953170308185, 04953170288968, 04953170308161, 04953170339264, 04953170308277, 04953170339394, 04953170308178, 04953170288876, 04953170308123, 04953170339196, 04953170062988, 04953170339974, 04953170063008, 04953170339998, & 04953170340147; All Serial Numbers.

Distribution Pattern:

US Nationwide distribution.

Voluntary or Mandated:

Voluntary: Firm initiated