FDA Medical devices recall ·
Halyard, MIDTOWN GENERAL ARTERIOGRAM recall
- Recall number
- Z-0928-2026
- Date
- (initiated November 14, 2025)
- Company / brand
- AVID Medical, Inc.
9000 Westmont Dr, Toano, VA, United States - Category
- Medical devices › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 300 units
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
Halyard, MIDTOWN GENERAL ARTERIOGRAM. Catalog Number: EUHM009-01.
Why was it recalled?
Potential for incomplete seal on header bag.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
Catalog Number: EUHM009-01. UDI-DI: 10809160346839. Lot Number: 1635477. Expiration Date: 5/29/2028.
Distribution
US distribution to GA, IL, NE, MD.
States: Georgia Illinois Maryland Nebraska
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (medical devices), recall Z-0928-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.