Class II
Medical Device Recall: Halyard KIT, CARDIAC ROBOTIC - Medical convenience kits Model Number: ESJH017-03
AVID Medical, Inc. · September 20, 2024
Reason for Recall
Sponge forceps and towel clamps associated with small loose metal flakes potentially could detach from the components. Metal flakes on components may enter a patients surgical site undetected causing local reactions or possible foreign body reactions
Distribution
US Nationwide distribution.
States Affected
NATIONWIDE
Quantity Affected
46 eaches
Source: FDA (openFDA Device Enforcement)
Recall number: Z-0392-2025
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.