Class II
Medical Device Recall: Halyard, MIDTOWN GENERAL ARTERIOGRAM. Catalog Number: EUHM009-01.
AVID Medical, Inc. · November 14, 2025
Reason for Recall
Potential for incomplete seal on header bag.
Distribution
US distribution to GA, IL, NE, MD.
States Affected
GA, IL, MD, NE
Quantity Affected
300 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-0928-2026
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.