← Search recalls
FDA (Device enforcement)Recalled 2024-03-07class ii

Olympus Corporation of the Americas: 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,

Hazard

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.

Details from the source

Reason for recall: 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. Distribution: Worldwide distribution - US Nationwide and the countries of AU, CA, HK, KR. Quantity: 150 units: (20 units US); (130 units OUS) Lot/code info: UDI-DI:00821925044579 Lot Code: CA179370

UPC codes

00821925044579

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

Hurt by this product? Start a free Case Check

ProductRisk is not a law firm and does not provide legal services or legal advice. ProductRisk is a free consumer product-safety information service operated by Plaintify, Inc., a technology company. If you ask to be connected with a law firm, any legal services are provided by that firm — not by ProductRisk or Plaintify.

Privacy · Plaintify