DeRoyal Industries Inc: Device Recall
Recall #Z-1291-2025 · 01/31/2025
Class II: Risk
Recall Details
- Recall Number
- Z-1291-2025
- Classification
- Class II
- Product Type
- Device
- Recalling Firm
- DeRoyal Industries Inc
- Status
- Ongoing
- Date Initiated
- 01/31/2025
- Location
- Powell, TN, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 714 cases
Reason for Recall
Due to the inner diameter of the suction tubing connector being smaller than the suction canister lid port connection. This size difference, combined with the durometer of the plastic material, makes the assembly to a suction canister lid port difficult. This could result in inadequate suction and cause a delay in patient care.
Product Description
DeRoyal REF 71-C5100NS Tubing, Suction, Connector; DeRoyal REF 71-C6100NS Tubing, Suction, Connector; DeRoyal REF 71-C7100NS Tubing, Suction, Connector Indicated use - Fluid Movement
Distribution Pattern
U.S.: IL, MN, NC, PA, and VA O.U.S.: N/A
Other Recalls by DeRoyal Industries Inc
- Class II: Risk 01/15/2025
- 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.