Olympus Corporation of the Americas: Medical Device Recall in 2022 - (Recall #: Z-1814-2022)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2022.

Data Source: FDA.

Product Description:

Olympus POWERSEAL 5MM, 37CM, CURVED JAW SEALER & DIVIDER, DOUBLE-ACTION Model Number: PS-0537CJDA. An electrosurgical device use in laparoscopic/minimally invasive or open surgical procedures.

Product Classification:

Class II

Date Initiated: August 12, 2022

Date Posted: October 5, 2022

Recall Number: Z-1814-2022

Event ID: 90788

Reason for Recall:

An out of specification component preventing the blue retention ring from keeping the rotation knob in place. This may result in a loose rotation collar and retention ring and cause delay of treatment

Status: Ongoing

Product Quantity: 231.4 units (5/box); 510 units (5/box) OUS

Code Information:

UDI-DI: 00821925044555 Lot Numbers: CA191233 CA191234 CA191235 CA233514 CA233515 CA233516 CA233517 CA233518 CA236206 CA236208 CA236213 CA236215 CA236216 CA236217 CA236220 CA236227 CA236228 CA236230 CA236238 CA236240 CA236243 CA236261 CA236272 CA236273 CA236276 CA236278 CA236290

Distribution Pattern:

Nationwide OUS: AUSTRALIA, CANADA , HONG KONG, CHINA, KOREA

Voluntary or Mandated:

Voluntary: Firm initiated