WhichRecall
Class IIReported 2025-12-24

Halyard, MIDTOWN GENERAL ARTERIOGRAM. Catalog Number: EUHM009-01.

Recalled by AVID Medical, Inc.

Reason for Recall

Potential for incomplete seal on header bag.

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Recall Number
Z-0928-2026
Classification
Class II
Status
Ongoing
Category
device
Initiated
2025-11-14
Reported
2025-12-24
Distribution
US distribution to GA, IL, NE, MD.
Code Info
Catalog Number: EUHM009-01. UDI-DI: 10809160346839. Lot Number: 1635477. Expiration Date: 5/29/2028.
Source: openFDA enforcement report. WhichRecall is not affiliated with the FDA. See our disclaimer.
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