AVID Medical recalls Halyard Arteriogram (EUHM009-01) due to potential incomplete seal on header bag. Affected units may have safety risks during medical procedures.
Potential for incomplete seal on header bag.
AVID Medical is recalling Halyard Arteriogram products (catalog number EUHM009-01) because the header bag might not seal properly. This could lead to safety issues during medical procedures if the seal fails.
The header bag may not seal completely, which could allow fluid leakage during medical procedures. This might cause contamination or other complications if the seal fails under pressure.
Medical professionals using Halyard Arteriogram products with catalog number EUHM009-01 are likely affected. Patients undergoing procedures with these devices may be at risk if the seal fails.
Check for catalog number EUHM009-01 on the product label. The product was sold with lot number 1635477 and expires May 29, 2028.
Look for catalog number EUHM009-01 on the product label to confirm if it is affected.
The recall indicates a potential risk, but the product is not unsafe unless the header bag seal fails. Affected units should be checked.
The recall does not specify a remedy, so check the product label for catalog number EUHM009-01 to determine if it is affected.
The product was sold with lot number 1635477 and expires May 29, 2028.
We’ve drafted a message you can send AVID Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0928-2026 — AVID Medical AVID Medical Hello, I own a AVID Medical that is covered by recall Z-0928-2026 from AVID Medical. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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.
