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Medical Device

Halyard, Drape Pack. Kit Code: LMDP36-01.

Recall date: 2026-06-17 · Source: FDA_DEVICE
Brand / Firm
AVID Medical, Inc.
Product
Halyard, Drape Pack. Kit Code: LMDP36-01.
Reason for recall
Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
Units affected
72 kits
Description
Halyard, Drape Pack. Kit Code: LMDP36-01.
View official recall notice →