Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Argyle Suction Tubing (Product # 8888301515) Argyle Suction Tubing is Recalled by Medtronic Minimally Invasive Therapies Group Due to Incorrect packaging. In one lot of Argyle Suction...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Medtronic Minimally Invasive Therapies Group directly.
Affected Products
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.
Quantity: 58,954
Why Was This 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.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Medtronic Minimally Invasive Therapies Group
Medtronic Minimally Invasive Therapies Group has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report