AVID Medical recalls Halyard EP LAB PK (Catalog ESJH009-03) due to potential incomplete seal on header bag. This could affect product integrity but no specific injury risk is mentioned.
Potential for incomplete seal on header bag.
AVID Medical is recalling Halyard EP LAB PK products (Catalog Number ESJH009-03) because the header bag might not seal properly. This could lead to product issues but the recall does not mention any injury risks.
The header bag might not seal completely, which could lead to product integrity issues. However, the recall does not specify any risk of injury or serious harm.
Users of Halyard EP LAB PK products with Catalog Number ESJH009-03 are affected. The risk is low as no injury mechanism is described.
Check for Halyard EP LAB PK products with Catalog Number ESJH009-03. The product also has UDI-DI: 10809160427316 and Lot Number 1653112.
Identify if your Halyard EP LAB PK has Catalog Number ESJH009-03, UDI-DI: 10809160427316, or Lot Number 1653112.
The recall does not mention any injury risk.
Check for Catalog Number ESJH009-03, UDI-DI: 10809160427316, or Lot Number 1653112.
The recall does not specify a remedy, so no action is required beyond checking product details.
We’ve drafted a message you can send AVID Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0927-2026 — AVID Medical AVID Medical Hello, I own a AVID Medical that is covered by recall Z-0927-2026 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.
