Class II

Medical Device Recall: smiths medical portex, Thermovent 1200, 15mm/22mm: a) REF 100/582/000; b) REF 100/582/000JP; c) REF 100/582/000JS

Smiths Medical ASD Inc. · July 18, 2024

Reason for Recall

Uncertainty in the seal integrity of the sterile packaging.

Distribution

Worldwide distribution.

Quantity Affected

141,196 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-0147-2025

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.