FDA Enforcement Class II Ongoing

POWERSEAL 5 mm, 44 cm, Curved Jaw Sealer and Divider, Double Action is indicated for use in general surgery and such surgical specialties as urologic, colorectal, bariatric, vascular, thoracic, and gynecologic. Model/Catalog Number: PS-0544CJDA

Recall: Z-1701-2024 · Reported May 8, 2024

Enforcement

Recall Number
Z-1701-2024
Event ID
94375
Classification
Class II
Status
Ongoing
Product Type
Devices
Firm
Olympus Corporation of the Americas
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Report Date
May 8, 2024
Initiation Date
March 7, 2024
Classification Date
April 30, 2024
Address
3500 Corporate Pkwy, Center Valley, PA, 18034-8229, United States

Description

POWERSEAL 5 mm, 44 cm, Curved Jaw Sealer and Divider, Double Action is indicated for use in general surgery and such surgical specialties as urologic, colorectal, bariatric, vascular, thoracic, and gynecologic. Model/Catalog Number: PS-0544CJDA

Reason

Upon initial activation of the seal function, the POWERSEAL non-conformance results in an immediate Incomplete Seal Cycle tone with the accompanying message on the generator screen, and no energy would be delivered to the device resulting in delay in surgery.

Code Info

UDI-DI:00821925044579 Lot Code: CA179370

Distribution

Worldwide distribution - US Nationwide and the countries of AU, CA, HK, KR.

Quantity

150 units: (20 units US); (130 units OUS)