Halyard, MIDTOWN GENERAL ARTERIOGRAM. Catalog Number: EUHM009-01.
Reported: December 24, 2025 Initiated: November 14, 2025 #Z-0928-2026
Product Description
Halyard, MIDTOWN GENERAL ARTERIOGRAM. Catalog Number: EUHM009-01.
Reason for Recall
Potential for incomplete seal on header bag.
Details
- Recalling Firm
- AVID Medical, Inc.
- Units Affected
- 300 units
- Distribution
- US distribution to GA, IL, NE, MD.
- Location
- Toano, VA
Frequently Asked Questions
What product was recalled? ▼
Halyard, MIDTOWN GENERAL ARTERIOGRAM. Catalog Number: EUHM009-01.. Recalled by AVID Medical, Inc.. Units affected: 300 units.
Why was this product recalled? ▼
Potential for incomplete seal on header bag.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on December 24, 2025. Severity: Moderate. Recall number: Z-0928-2026.
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