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Recall database

AVID Medical, Inc. recalls

Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.

Showing 1–12 of 52 recalls

Class IIOngoingZ-2410-2026

AVID Medical, Inc. recalls Halyard

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

AVID Medical, Inc.VAJun 17, 2026

Class IIOngoingZ-2409-2026

AVID Medical, Inc. recalls Halyard

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

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.

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.

AVID Medical, Inc.VAJun 17, 2026

Class IOngoingZ-1979-2026

AVID Medical, Inc. recalls Halyard VA DETROIT CATH LAB PACK kit. Model Numbers: VMCD029.

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.

AVID Medical, Inc.VAMay 13, 2026

Class IOngoingZ-1978-2026

AVID Medical, Inc. recalls Halyard SAMMC ANGIOGRAPHY kit. Model Numbers: SAMM066-15.

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.

AVID Medical, Inc.VAMay 13, 2026

Class IOngoingZ-1977-2026

AVID Medical, Inc. recalls Halyard PERC TRAY kit. Model Numbers: SLPC34-01

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.

AVID Medical, Inc.VAMay 13, 2026

Class IOngoingZ-1976-2026

AVID Medical, Inc. recalls Halyard NEURO IR PERIPHERAL (PS 64405) kit. Model Number: UINR44-01.

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.

AVID Medical, Inc.VAMay 13, 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.

AVID Medical, Inc.VAMay 13, 2026

Class IOngoingZ-1974-2026

AVID Medical, Inc. recalls Halyard CATH LAB kit. Model Number: SACL75-01.

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.

AVID Medical, Inc.VAMay 13, 2026

Class IOngoingZ-1973-2026

AVID Medical, Inc. recalls Halyard CATH LAB kit. Model Number: SACL75AM.

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.

AVID Medical, Inc.VAMay 13, 2026

Class IOngoingZ-1972-2026

AVID Medical, Inc. recalls Halyard CARDIAC CATH TRAY SHANDS JAX kit. Model Number: SHND401-04

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.

AVID Medical, Inc.VAMay 13, 2026