Z-2719-2026 Class II Ongoing

Recalled by Olympus Corporation of the Americas — Center Valley, PA

FDA device recall Z-2719-2026 was initiated by Olympus Corporation of the Americas on May 5, 2026 and is designated Class II. Reason for recall: Some sterilization parameters included in the IFU may not consistently render the devices adequately sterile and therefore should no longer be used to sterilize the devices. The recall status is ongoing. Affected quantity: 1,156 units.

Recall Details

Product Type
Devices
Report Date
July 22, 2026
Initiation Date
May 5, 2026
Termination Date
N/A
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
1,156 units

Product Description

Olympus Toomey Evacuator 50cc with Adaptor. Model Number: 188A.

Reason for Recall

Some sterilization parameters included in the IFU may not consistently render the devices adequately sterile and therefore should no longer be used to sterilize the devices.

Distribution Pattern

Worldwide distribution - US Nationwide and the countries of Canada, Japan, EU, and Latin America.

Code Information

Model Number: 188A. UDI-DI: 00821925001077. All Lot Numbers