Reported Dec 24, 2025 · Ongoing
Halyard, MIDTOWN GENERAL ARTERIOGRAM. Catalog Number: EUHM009-01.
AVID Medical, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: AVID Medical, Inc. · 9000 Westmont Dr · Toano, VA · 23168-9351
Is this the product you have?
- Halyard, MIDTOWN GENERAL ARTERIOGRAM
- Catalog NumberEUHM009-01
- Lot codes and dates
- Catalog NumberEUHM009-01
- UDI-DI10809160346839
- Lot Number1635477
- Expiration Date5/29/2028
- Amount recalled
- 300 units
This recall covers 5 products
The agency filed one notice per product. You are reading one of them; the other 4 are below.
Where it was sold
Why it was recalled
Potential for incomplete seal on header bag.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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