Recall
FDAHealthApril 30, 2026

AVID Medical, Inc. — Halyard, Drape Pack. Kit Code: LMDP36-01.

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

Is this relevant to me?

Geography
Nationwide
Source agency
FDA
Category
Health
Published
April 30, 2026

US Nationwide distribution in the state of Iowa.

What's affected?

Product
Halyard, Drape Pack. Kit Code: LMDP36-01.
Lot code
LMDP36-01

Additional details

Kit Code: LMDP36-01.UDI-DI: 10809160479148. Lot Number: LMDP36-01. Expiration Date: 9/10/2028

What should I do?

Recommended action

Class II recall. Voluntary: Firm initiated Quantity affected: 72 kits.

View original FDA notice →

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