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FDA · Medical devices ·

Halyard STANDARD LINE INSERTION PACK recall

AVID Medical, Inc. recalled Halyard STANDARD LINE INSERTION PACK on July 29, 2026 because of defects in the silicone seal, which may result in "doming" of the silicone seal due to improper sealing, potentially leading to fluid occlusion or leakage. It was sold nationwide.

Why it was recalled

Defects in the silicone seal, which may result in "doming" of the silicone seal due to improper sealing, potentially leading to fluid occlusion or leakage.

What's recalled

Halyard STANDARD LINE INSERTION PACK. Model/Catalog Number: PVHM234-01. Convenience kit.

Quantity: 112 kits

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
U.S. Nationwide distribution in the state of California.
Status
Ongoing
Recall number
Z-2772-2026
Source
U.S. Food and Drug Administration

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