AVID Medical recalls Halyard Eye Bag Pack (Kit Code UIEB48-01) due to unsterilized pouches that could pose infection risks. Affected units include specific lot numbers and expiration dates.
Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
AVID Medical is recalling Halyard Eye Bag Packs with Kit Code UIEB48-01 because some pouches were not properly sterilized. This could lead to infection risks if used for medical purposes. The recall affects specific lot numbers and expiration dates.
The pouches were distributed without proper sterilization, which could lead to infection if used in medical procedures. This is a contamination risk rather than a physical hazard.
Patients using Halyard Eye Bag Packs with Kit Code UIEB48-01 for medical procedures are most at risk. The recall applies to specific lot numbers and expiration dates.
Check for Kit Code UIEB48-01 on the product. The lot number is UIEB48-01 and expiration date is August 7, 2028.
Look for Kit Code UIEB48-01, lot number UIEB48-01, and expiration date August 7, 2028 on the Halyard Eye Bag Pack.
The pouches were distributed without proper sterilization, which could lead to infection risks if used in medical procedures.
Check the product for Kit Code UIEB48-01, lot number UIEB48-01, and expiration date August 7, 2028. If you have these details, contact AVID Medical for further instructions.
The recall is for unsterilized pouches that could cause infection, not a physical hazard like injury or fire.
We’ve drafted a message you can send AVID Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2410-2026 — AVID Medical AVID Medical Hello, I own a AVID Medical that is covered by recall Z-2410-2026 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.