{"url_path":"/fda/device/recalls/Z-2772-2026","section_key":"summary","section_title":"DEVICE Recall: AVID Medical, Inc. — Halyard STANDARD LINE INSERTION PACK. Model/Catalog Number: PVHM234-01.     Convenience kit.","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-05-19","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2772-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"AVID Medical, Inc."},"word_count":89,"has_tables":false,"body_markdown":"# FDA DEVICE Recall: Z-2772-2026\n\n**Recalling firm:** AVID Medical, Inc.\n**Classification:** Class II\n**Status:** Ongoing\n**Type:** Voluntary: Firm initiated\n**Initiated:** 2026-05-19\n**Report date:** 2026-07-29\n\n## Product\nHalyard STANDARD LINE INSERTION PACK. Model/Catalog Number: PVHM234-01.     Convenience kit.\n\n## Reason\nDefects in the silicone seal, which may result in \"doming\" of the silicone seal due to improper sealing, potentially leading to fluid occlusion or leakage.\n\n## Affected lots\nModel/Catalog Number: PVHM234-01. UDI-DI: 10809160416761. Lot Numbers (Expiration date): 1597314 (8/31/2026), 1599022 (5/31/2026).\n\n## Distribution\nU.S. Nationwide distribution in the state of California."}