Class II
Medical Device Recall: ENT RES, 100 ML, Non-Sterile W CLAMP & FEMALE LUER, Product Code 68-2231-28
Smiths Medical ASD Inc. · June 26, 2024
Reason for Recall
Certain CADD Medication Cassette Reservoirs may exhibit a weakened weld joint between the medication bag and tubing due to a production equipment malfunction. This could result in a medication leakage.
Distribution
Worldwide distribution.
Quantity Affected
120960 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-0018-2025
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.