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AVID Medical, Inc. recalls Halyard, MIDTOWN GENERAL ARTERIOGRAM. Catalog Number: EUHM009-01.
Recalled December 24, 2025 · FDA recall Z-0928-2026 · AVID Medical
Hazard
Potential for incomplete seal on header bag. · FDA Class II
Units
300 units
Sold at
US distribution to GA, IL, NE, MD.
Description
Potential for incomplete seal on header bag.
Product
Halyard, MIDTOWN GENERAL ARTERIOGRAM. Catalog Number: EUHM009-01.
Manufacturer(s)
AVID Medical, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →