Medtronic Minimally Invasive Therapies Group recalls Argyle Suction Tubing (Product # 8888301515) Argyle Suction Tubing is an extruded tube used as an extension for differe…

Recall date

October 24, 2017

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-0936-2018

FDA classification

Class II

Brand / firm

Medtronic Minimally Invasive Therapies Group

Sold / distributed

USA (nationwide) Distribution

Why it was recalled

Incorrect packaging. In one lot of Argyle Suction Tubing, the pouch may be incorrectly labeled as the Salem Sump Dual Lumen Stomach Tube. This product may have been distributed within the case of Argyle Suction Tubing.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Argyle Suction Tubing (Product # 8888301515) Argyle Suction Tubing is an extruded tube used as an extension for different types of devices in an operating room, bonded with 2 female sure grip connectors at each end of the tube to facilitate the plug/ insertion of the device and also includes a male connector that can be used for devices designed with female connectors, This product is sterile, non-conductive and latex free.