Avid Medical, Inc.
Avid Medical, Inc. holds FDA 510(k) medical device clearances, cleared in 2000, with 203 FDA device recalls on record.
Top product codes for Avid Medical, Inc.
FDA recalls by Avid Medical, Inc.
10 most recent of 203- Z-0283-2027 — Halyard ANTERIOR HIP PACK. Model/Catalog Number: SOAH30.
- Z-0282-2027 — Halyard ANTERIOR HIP PACK. Model/Catalog Number: SOAH31.
- Z-3151-2026 — Haylard 18G SINGLE SHOT EPI TRAY; Model/Item Number (Kit): DPGE002-02;
- Z-3154-2026 — Haylard UNIV IMAGING BIOPSY TRUCUSTOM; Model/Item Number (Kit): VARV042-03;
- Z-3153-2026 — Haylard BASIC BIOPSY TRAY; Model/Item Number (Kit): PM415;
- Z-3152-2026 — Haylard CONTINUOUS NERVE BLOCK TRAY; Model/Item Number (Kit): BMCN001-05;
- Z-0098-2027 — ROBOTIC PROSTATECTOMY PACK; Model/Item Number (Kit): NAMC423-11;
- Z-0094-2027 — ADULT HEART TRAY SHANDS JACKS; Model/Item Number (Kit): SHND419-08;
- Z-0096-2027 — CRANIOTOMY PACK; Model/Item Number (Kit): WRNM035-20;
- Z-0103-2027 — UROLOGY MAJOR; Model/Item Number (Kit): WRNM058-10;
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.