Class I
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 are contaminated with Aspergillus penicillioides
Distribution
US Nationwide distribution in the state of NE.
States Affected
NATIONWIDE
Quantity Affected
288 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-3108-2026
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.