AVID Medical recalls Halyard Pain Pack Kit Code AMPK48-01 due to unsterilized pouches. Affected units may pose infection risks if used without proper sterilization.
Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
AVID Medical is recalling Halyard Pain Pack kits with specific codes because some pouches were not properly sterilized. Using these kits could lead to infections if the pouches are not sterilized correctly.
The recalled pouches were distributed without proper sterilization. This means they might not be safe for medical use and could lead to infections if used without proper sterilization.
Patients using the Halyard Pain Pack kit with code AMPK48-01 are affected. Those who have the kit may be at risk of infection if the pouches are not sterilized properly.
Check for the kit code AMPK48-01 on the product. The lot number is 334669 and expiration date is August 27, 2028.
Look for the kit code AMPK48-01 on the product to confirm if it is recalled.
The product was recalled because some pouches were distributed without proper sterilization.
Using the unsterilized pouches could lead to infections if not properly sterilized.
Check for the kit code AMPK48-01, lot number 334669, and expiration date August 27, 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-2407-2026 — AVID Medical AVID Medical Hello, I own a AVID Medical that is covered by recall Z-2407-2026 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.
