Medical device recalls Moderate risk

AVID Medical, Inc. recalls Halyard, GENERAL LAPAROSCOPY PACK. Catalog Number: VAST018-10.

Recall date
November 14, 2025
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-0926-2026
FDA classification
Class II
Brand / firm
AVID Medical, Inc.
Sold / distributed
US distribution to GA, IL, NE, MD.

Why it was recalled

Potential for incomplete seal on header bag.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Halyard, GENERAL LAPAROSCOPY PACK. Catalog Number: VAST018-10.

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