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Medtronic Minimally Invasive Therapies Group recalls Argyle Suction Tubing (Product # 8888301515) Argyle Suction Tubing is an extruded tube used as an extension for diff
Recalled March 21, 2018 · FDA recall Z-0936-2018 · Medtronic Minimally Invasive Therapies Group
Hazard
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. · FDA Class II
Units
58,954
Sold at
USA (nationwide) Distribution
Description
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.
Product
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.
Manufacturer(s)
Medtronic Minimally Invasive Therapies Group
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →