Olympus Corporation of the Americas: Medical Device Recall in 2026 - (Recall #: Z-1453-2026)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2026.

Data Source: FDA.

Product Description:

Olympus Inner Sheath 21 Fr. Model No. A2660T. for endoscopic diagnosis and treatment in urological applications.

Product Classification:

Class II

Date Initiated: November 11, 2025

Date Posted: March 4, 2026

Recall Number: Z-1453-2026

Event ID: 98288

Reason for Recall:

Complaints of the ceramic tip of the resection sheath breaking have been received.

Status: Ongoing

Product Quantity: 1 unit

Code Information:

Model No. A2660T; UDI: 04042761004183; All Lots.

Distribution Pattern:

US Nationwide Distribution.

Voluntary or Mandated:

Voluntary: Firm initiated