Class II

Medical Device Recall: Halyard TRANSPORT BAG KIT. Kit Code: LIFE0080-01.

AVID Medical, Inc. · January 2, 2026

Reason for Recall

Tyvek bag seal issue which may compromise sterility of the kit.

Distribution

US Nationwide distribution in the states of New Jersey.

States Affected

NATIONWIDE

Quantity Affected

1,500 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1338-2026

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.