Class II

Medical Device Recall: smiths medical portex, Y' PIECE 15MM, REF 100/276/000

Smiths Medical ASD Inc. · July 18, 2024

Reason for Recall

Uncertainty in the seal integrity of the sterile packaging.

Distribution

Worldwide distribution.

Quantity Affected

9,133 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-0145-2025

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.