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.
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: 160 units: (20 units US); (140 units OUS) Lot/code info: UDI-DI: 00821925044531 Lot number: CA182554
00821925044531
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.