Lower riskMedical device recall · FDA · Published November 14, 2025
AVID Medical Halyard Arteriogram Recall: Potential Incomplete Seal Hazard
AVID Medical recalls Halyard Arteriogram (EUHM009-01) due to potential incomplete seal on header bag. Affected units may have safety risks during medical procedures.
“AVID Medical Halyard Arteriogram Recall: Potential Incomplete Seal Hazard.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/50652-avid-medical-halyard-arteriogram-recall-potential-incomplete-seal-hazard. Based on FDA recall #Z-0928-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0928-2026%22&limit=1).
The FDA announced on Nov. 14, 2025, that AVID Medical, Inc. is recalling Halyard and MIDTOWN GENERAL ARTERIOGRAM arterial catheters due to a potential for an incomplete seal on the header bag. The agency issued recall number Z-0928-2026 for the Class II voluntary recall.
How to tell if you have it
Brand: AVID Medical
Product names: Halyard, MIDTOWN GENERAL ARTERIOGRAM
Catalog Number: EUHM009-01
Lot Number: 1635477
Expiration Date: 5/29/2028
Units affected: 300
The hazard
The recall addresses the potential for an incomplete seal on the header bag of the arterial catheters, according to the FDA.
Context
GovInfoNow's records show AVID Medical, Inc. has 23 other recalls on record since June 22, 2017. Recent brand recalls include a July 22, 2026, recall of Halyard IV START KIT NON-STERILE kits for open seals and an Aug. 10, 2026, recall of Haylard Continuous Nerve Block Trays for sterility risks in sodium chloride ampules. Other recent recalls of similar products include the Mozarc Medical Acute High Pressure Catheter Tray Recall (Oct. 17, 2025), the Mozarc Medical Acute High Pressure Catheter Tray Extensions Recall (Oct. 17, 2025), and the Merit Medical Allwell Angioplasty Pack Recall (Dec. 4, 2025).
How to tell if you have this one
Check for catalog number EUHM009-01 on the product label. The product was sold with lot number 1635477 and expires May 29, 2028.
Brand
AVID Medical
Category
Medical device
FDA recall event · 5 products
All 5 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
Classification
Class II
Status
Ongoing
Distribution
US distribution to GA, IL, NE, MD.
Recall number
Product, codes & lots
Quantity
Z-0926-2026
Halyard, GENERAL LAPAROSCOPY PACK. Catalog Number: VAST018-10.; Catalog Number: VAST018-10. UDI-DI: 10809160452257. Lot Number: 1651776. Expiration Date: 3/12/2027
42 units
Z-0927-2026
Halyard, EP LAB PK. Catalog Number: ESJH009-03.; Catalog Number: ESJH009-03. UDI-DI: 10809160427316. Lot Code: Lot Number: 1653112. Expiration Date: 5/28/2028.
240 units
Z-0928-2026
Halyard, MIDTOWN GENERAL ARTERIOGRAM. Catalog Number: EUHM009-01.; Catalog Number: EUHM009-01. UDI-DI: 10809160346839. Lot Number: 1635477. Expiration Date: 5/29/2028.
300 units
Z-0929-2026
Halyard, MAJOR PACK. Catalog Number: JEMJ10-01.; Catalog Number: JEMJ10-01. UDI-DI: 10809160443217. Lot Number: 1635770. Expiration Date: 7/26/2027.
90 units
Z-0930-2026
Halyard, HEAD AND NECK TRAY. Catalog Number: EURO016-09.; Catalog Number: EURO016-09. UDI-DI: 10809160461198. Lot Number: 1655501 Expiration Date: 3/31/2027.
56 units
Based on the official FDA remedy
What to do — step by step
Check Product Label
Look for catalog number EUHM009-01 on the product label to confirm if it is affected.
Where it went and when
Where it was distributed
Distributed in 4 states.
Listed by the agency
Not listed
FDA distribution: “US distribution to GA, IL, NE, MD.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Georgia, Illinois, Maryland, Nebraska.
Recall timeline
FDA published this recall 40 days after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-0928-2026 (November 14, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0928-2026 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.