Official recall notice

FDA DeviceClass IINotable

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

Recall date
2026-06-17
FDA class
Class II

Why it was recalled

Hazard

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

Recommended action

What to do

72 kits

Product description

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

Verify with the official notice →
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