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Parker Quality & Compliance

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Device recall

Halyard MINOR PACK. Model/Catalog Number: VASF105-08.

FDA recall source

Recall number
Z-0331-2027
Event id
99967
Status
Open, Classified
FDA classification
Class II
Recalling firm
AVID Medical, Inc.
Posted
Nov 3, 2026
Initiated
Sep 8, 2026
Product code
LRO
Device type
General Surgery Tray
Reason
Potential for open seals on header bags, compromising sterility.
Root cause
Process control
Quantity
108 kits
Code info
Model/Catalog Number: VASF105-08. UDI-DI: 10809160451960. Lot Number: 1659384. Expiration Date: 9/30/2027.
Distribution
U.S Nationwide distributor in the state of Illinois.
Location
Toano, VA