Avid Medical, Inc.
Avid Medical, Inc. holds FDA 510(k) medical device clearances, cleared in 2000, with 178 FDA device recalls on record.
Top product codes for Avid Medical, Inc.
FDA recalls by Avid Medical, Inc.
10 most recent of 178- Z-3109-2026 — Halyard IV Start Kit Non-Sterile REF: KRIV26-02
- Z-2964-2026 — Halyard LAVH PACK, Model/Catalog Number: USAR053-11 containing Clearify Visualization System (5303907).
- Z-3006-2026 — Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03
- Z-3005-2026 — Brand Name: Halyard Product Name: DAVINCI TRUCUSTOM BUNDLE containing TRAY FOLEY 16FR W/STATLOCK Model/Catalog Number: SAMM064-27
- Z-3011-2026 — Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03
- Z-3009-2026 — Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03
- Z-3010-2026 — Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03
- Z-3008-2026 — Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03
- Z-3007-2026 — Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03
- Z-2772-2026 — Halyard STANDARD LINE INSERTION PACK. Model/Catalog Number: PVHM234-01. Convenience kit.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Avid Medical, Inc.
Data sourced from openFDA. This site is unofficial and independent of the FDA.