FDA recall record

AVID Medical Halyard STANDARD LINE INSERTION PACK recall — FDA Z-2772-2026

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.

Class IIclassification
Z-2772-2026official record ID
Jul 29, 2026report date

Recall record at a glance

Official recordZ-2772-2026
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmAVID Medical, Inc.
Report dateJul 29, 2026
Recall initiation dateMay 19, 2026
Quantity112 kits
LocationToano, VA, United States

Official product description

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

Why the product 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.

Distribution information

U.S. Nationwide distribution in the state of California.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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