FDA DeviceClass IINotable

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

Date: 2026-06-17
Brand: AVID Medical, Inc.
Category: Medical Device
FDA Class: Class II

Description

Inadvertent distribution of sealed pouches that had not undergone validated sterilization.

Hazard

Inadvertent distribution of sealed pouches that had not undergone validated sterilization.

Remedy

72 kits

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