Class II

Medical Device Recall: Halyard IV Start Kit Non-Sterile REF: KRIV26-02

AVID Medical, Inc. · July 14, 2026

Reason for Recall

Convenience kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which lacks sterility assurance due to to wrinkles in the paper lidding which may breach the seal area.

Distribution

US Nationwide distribution in the state of NE.

States Affected

NATIONWIDE

Quantity Affected

98 Kits

Source: FDA (openFDA Device Enforcement)

Recall number: Z-3109-2026

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.

AVID Medical, Inc. Medical Device Recall: Halyard IV Start Kit Non-Sterile REF: KRIV26-02 | SafeCheck