Class II

Medical Device Recall: CADD Medication Cassette Reservoir, 50mL, FS, Product Code 21-7301-24

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

119535 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-0013-2025

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.

Smiths Medical ASD Inc. Medical Device Recall: CADD Medication Cassette Reservoir, 50mL, FS, Product Code 21-7301-24 | SafeCheck