Olympus Corporation of the Americas: Medical Device Recall in 2026 - (Recall #: Z-1437-2026)

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 Cystoscope Outer Sheath; Model/Catalog number: WA22810A;

Product Classification:

Class II

Date Initiated: September 13, 2024

Date Posted: March 4, 2026

Recall Number: Z-1437-2026

Event ID: 98300

Reason for Recall:

Product being removed due to incompatibility when used in conjunction with a GreenLight Laser for BPH therapy which could damage the tip of the device.

Status: Ongoing

Product Quantity: 633 units

Code Information:

Model: WA2280A; UDI: 04042761051729; Lot#: All lots;

Distribution Pattern:

Distribution US nationwide.

Voluntary or Mandated:

Voluntary: Firm initiated