Medtronic recalls Valleylab Laparoscopic Flexible Laparoscopic Argon Electrodes Item Code: E253028 The Valleylab Laparoscopic Handset an

Recalled August 24, 2016 · FDA recall Z-2554-2016 · Medtronic

Hazard

Potential for compromise of the package resulting in a breach of the sterile barrier · FDA Class II

Units

13420

Sold at

Worldwide Distribution - US (nationwide) and Internationally to Australia, Canada, Japan, Korea, Hong Kong, Thailand,

Description

Potential for compromise of the package resulting in a breach of the sterile barrier

Product

Valleylab Laparoscopic Flexible Laparoscopic Argon Electrodes Item Code: E253028 The Valleylab Laparoscopic Handset and Electrodes are indicated for use in laparoscopic and thoracoscopic surgical procedures where the delivery of electrosurgical current, irrigation and suction via a single handset is desirable

Manufacturer(s)

Medtronic

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →