Class II

Medical Device Recall: DeRoyal AMG Suction Connector Tubing REF: 71-2083, 71-C506, 71-C510, 71-C512, 71-C520, Tubing is intended for fluid movement

DeRoyal Industries Inc · January 15, 2025

Reason for Recall

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.

Distribution

U.S.: ND, NY, VA, WV, NJ, TN, OK, TN, GA, OH, MN, AZ, WI, IL, MA, MD, MO, AR, MS, NY, MS, SC, HI, AR, UT, HI, O.U.S.: Kuwait

States Affected

AR, AZ, GA, HI, IL, MA, MD, MN, MO, MS, ND, NJ, NY, OH, OK, SC, TN, UT, VA, WI, WV

Quantity Affected

224,770 tubes/connectors

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1174-2025

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.