AVID Medical recalls Halyard Drape Pack Kit (Code LMDP36-01) due to unsterilized pouches. Affected units may pose infection risks if used.
Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
AVID Medical is recalling Halyard Drape Pack Kit Code LMDP36-01 because some pouches were not properly sterilized. Using these pouches could lead to infection risks if they are used in medical procedures.
The pouches in this kit were distributed without proper sterilization. If used in medical procedures, they could introduce infections into patients.
Healthcare professionals using the Halyard Drape Pack Kit for medical procedures are most at risk. Patients using unsterilized pouches could face infection.
Check for the kit code LMDP36-01 on the product. The expiration date is September 10, 2028, and the lot number is LMDP36-01.
Look for the kit code LMDP36-01, expiration date 9/10/2028, and lot number LMDP36-01 on the product.
Yes, unsterilized pouches could lead to infection risks if used in medical procedures.
Check for kit code LMDP36-01, expiration date 9/10/2028, and lot number LMDP36-01.
The recall does not specify a remedy, so contact AVID Medical for guidance.
We’ve drafted a message you can send AVID Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2409-2026 — AVID Medical AVID Medical Hello, I own a AVID Medical that is covered by recall Z-2409-2026 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.
