DeRoyal Industries Inc: Device Recall
Recall #Z-1174-2025 · 01/15/2025
Class II: Risk
Recall Details
- Recall Number
- Z-1174-2025
- Classification
- Class II
- Product Type
- Device
- Recalling Firm
- DeRoyal Industries Inc
- Status
- Ongoing
- Date Initiated
- 01/15/2025
- Location
- Powell, TN, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 224,770 tubes/connectors
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.
Product Description
DeRoyal AMG Suction Connector Tubing REF: 71-2083, 71-C506, 71-C510, 71-C512, 71-C520, Tubing is intended for fluid movement
Distribution Pattern
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
Other Recalls by DeRoyal Industries Inc
- Class II: Risk 01/31/2025
- Class II: Risk 10/03/2024
- Class II: Risk 10/03/2024
- Class II: Risk 10/03/2024
- Class II: Risk 10/03/2024
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.