Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0936-2018 — 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 m

U.S. FDA — Device Enforcement · United States · 2017-10-24 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0936-2018
Date of alert
2017-10-24
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Medtronic Minimally Invasive Therapies Group
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
8888301515
Reported risk: 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.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.