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

Recall Z-1174-2025 — DeRoyal AMG Suction Connector Tubing REF: 71-2083, 71-C506, 71-C510, 71-C512, 71-C520, Tubing is intended for fluid movement

U.S. FDA — Device Enforcement · United States · 2025-01-15 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1174-2025
Date of alert
2025-01-15
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
DeRoyal Industries Inc
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00749756578981
Reported risk: The tubing may not ensure that the yankauer stays intact, and secure to the tubing / yankauer connection for a tight seal. This could result in inadequate suction and cause delay in patient care.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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