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AVID Medical, Inc. recalls

The FDA has posted 52 enforcement recalls from AVID Medical, Inc. since 2025, including 13 Class I (most serious) recalls. Most recent report: Jun 17, 2026.

Class I: 13Class II: 39

Latest recalls

View all 52 in the recall browser →
Class IIOngoingZ-2409-2026

AVID Medical, Inc. recalls Halyard

Inadvertent distribution of sealed pouches that had not undergone validated sterilization.

  • Orthopedic Tray
  • Process control
AVID Medical, Inc.VAJun 17, 2026
Class IIOngoingZ-2410-2026

AVID Medical, Inc. recalls Halyard

Inadvertent distribution of sealed pouches that had not undergone validated sterilization.

  • Orthopedic Tray
  • Process control
AVID Medical, Inc.VAJun 17, 2026
Class IIOngoingZ-2407-2026

AVID Medical, Inc. recalls Halyard

Inadvertent distribution of sealed pouches that had not undergone validated sterilization.

  • Orthopedic Tray
  • Process control
AVID Medical, Inc.VAJun 17, 2026
Class IIOngoingZ-2408-2026

AVID Medical, Inc. recalls Halyard

Inadvertent distribution of sealed pouches that had not undergone validated sterilization.

  • General Surgery Tray
  • Process control
AVID Medical, Inc.VAJun 17, 2026
Class IOngoingZ-1975-2026

AVID Medical, Inc. recalls Halyard HEART CATH

Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.

  • Cardiovascular Procedure Kit
  • Under Investigation by firm
AVID Medical, Inc.VAMay 13, 2026

Firm name as filed with the FDA: “AVID Medical, Inc.”. Related firm entities may file under separate names. Source: U.S. FDA openFDA device enforcement reports. Informational only — verify with the FDA before acting.