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AVID Medical, Inc. recalls Halyard, Drape Pack. Kit Code: LMDP36-01.
Recalled June 17, 2026 · FDA recall Z-2409-2026 · AVID Medical
Hazard
Inadvertent distribution of sealed pouches that had not undergone validated sterilization. · FDA Class II
Units
72 kits
Sold at
US Nationwide distribution in the state of Iowa.
Description
Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
Product
Halyard, Drape Pack. Kit Code: LMDP36-01.
Manufacturer(s)
AVID Medical, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →