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FDA · Medical devices ·

Halyard LAVH PACK, Model/Catalog Number recall

AVID Medical, Inc. recalled Halyard LAVH PACK, Model/Catalog Number on August 26, 2026 because of the kit component was subjected to EO sterilization, contrary to the manufacturer recommendation, which may have led to the component leaking in a kit. It was sold nationwide.

Why it was recalled

The kit component was subjected to EO sterilization, contrary to the manufacturer recommendation, which may have led to the component leaking in a kit.

What's recalled

Halyard LAVH PACK, Model/Catalog Number: USAR053-11 containing Clearify Visualization System (5303907).

Quantity: 40 packs

What to do

Check whether you have the product (match the lot numbers, dates or codes in the official notice). Stop using it, and return it or throw it away as the notice says.

Read the official FDA notice

Details

Company
AVID Medical, Inc., Toano, VA
Date
Severity
Class II
the product could cause temporary or reversible health problems.
Where sold
Nationwide
US Nationwide distribution in the state of TX.
Status
Ongoing
Recall number
Z-2964-2026
Source
U.S. Food and Drug Administration

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