Class II
Medical Device Recall: Halyard LAVH PACK, Model/Catalog Number: USAR053-11 containing Clearify Visualization System (5303907).
AVID Medical, Inc. · July 10, 2026
Reason for Recall
The kit component was subjected to EO sterilization, contrary to the manufacturer recommendation, which may have led to the component leaking in a kit.
Distribution
US Nationwide distribution in the state of TX.
States Affected
NATIONWIDE
Quantity Affected
40 packs
Source: FDA (openFDA Device Enforcement)
Recall number: Z-2964-2026
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.