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

View all recalls by DeRoyal Industries Inc →

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.