WhichRecall
Class IIReported 2026-02-11

Brand Name: Single Use Electrosurgical Knife KD-645 Product Name: Olympus Single Use Electrosurgical Knife KD-645 Model/Catalog Number: KD-645L Product Description: An electrosurgical device consisting of a handpiece with mechanical and/or electrical controls, and a monopolar electrode, intended to deliver a current from a system generator directly to tissues for cutting/coagulation/ablation during endoscopic (including laparoscopic, arthroscopic) surgery.

Recalled by Olympus Corporation of the Americas

Reason for Recall

A deterioration of the cutting knife, including overheating and burning, can contribute to tip breakage during use.

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Recall Number
Z-1223-2026
Classification
Class II
Status
Ongoing
Category
device
Initiated
2024-02-17
Reported
2026-02-11
Distribution
US Nationwide distribution.
Code Info
Model/Catalog Number: KD-645L UDI: 04953170407857 Lot Number(s): 2ZK, 31K, 32K, 33K, 35K, 3XK, 3YK, 3ZK, 42K, 43K, 44K, 45K, 46K, 47K, 48K, 49K, 4XK, 4YK, 4ZK, 51K, 52K, 53K, 54K, 55K, 56K, 57K, 58K, 59K
Source: openFDA enforcement report. WhichRecall is not affiliated with the FDA. See our disclaimer.
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