Class II

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

AVID Medical, Inc. · May 19, 2026

Reason for Recall

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

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

States Affected

NATIONWIDE

Quantity Affected

112 kits

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2772-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.