AVID Medical recalls

14 recent recalls on record for AVID Medical in CPSC, NHTSA, and FDA data as of July 24, 2026 at 3:00 AM UTC.

Models with recalls

Halyard (4)Halyard CARDIAC CATH PACK SAN23CARDQ kit (1)Halyard CARDIAC CATH PACK kit (1)Halyard CARDIAC CATH TRAY SHANDS JAX kit (1)Halyard CATH LAB kit (2)Halyard HEART CATH (1)Halyard NEURO IR PERIPHERAL (PS 64405) kit (1)Halyard PERC TRAY kit (1)Halyard SAMMC ANGIOGRAPHY kit (1)Halyard VA DETROIT CATH LAB PACK kit (1)

All AVID Medical recalls

FDA Class II · Medical device · June 17, 2026

Halyard recall — AVID Medical, Inc.

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

Official ID Z-2410-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Halyard recall — AVID Medical, Inc.

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

Official ID Z-2409-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Halyard recall — AVID Medical, Inc.

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

Official ID Z-2408-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Halyard recall — AVID Medical, Inc.

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

Official ID Z-2407-2026 · Official record ↗

FDA Class I · Medical device · May 13, 2026

Halyard VA DETROIT CATH LAB PACK kit recall — AVID Medical, Inc.

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.

Official ID Z-1979-2026 · Official record ↗

FDA Class I · Medical device · May 13, 2026

Halyard SAMMC ANGIOGRAPHY kit recall — AVID Medical, Inc.

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.

Official ID Z-1978-2026 · Official record ↗

FDA Class I · Medical device · May 13, 2026

Halyard PERC TRAY kit recall — AVID Medical, Inc.

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.

Official ID Z-1977-2026 · Official record ↗

FDA Class I · Medical device · May 13, 2026

Halyard NEURO IR PERIPHERAL (PS 64405) kit recall — AVID Medical, Inc.

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.

Official ID Z-1976-2026 · Official record ↗

FDA Class I · Medical device · May 13, 2026

Halyard HEART CATH recall — AVID Medical, Inc.

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.

Official ID Z-1975-2026 · Official record ↗

FDA Class I · Medical device · May 13, 2026

Halyard CATH LAB kit recall — AVID Medical, Inc.

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.

Official ID Z-1974-2026 · Official record ↗

FDA Class I · Medical device · May 13, 2026

Halyard CATH LAB kit recall — AVID Medical, Inc.

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.

Official ID Z-1973-2026 · Official record ↗

FDA Class I · Medical device · May 13, 2026

Halyard CARDIAC CATH TRAY SHANDS JAX kit recall — AVID Medical, Inc.

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.

Official ID Z-1972-2026 · Official record ↗

FDA Class I · Medical device · May 13, 2026

Halyard CARDIAC CATH PACK SAN23CARDQ kit recall — AVID Medical, Inc.

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.

Official ID Z-1971-2026 · Official record ↗

FDA Class I · Medical device · May 13, 2026

Halyard CARDIAC CATH PACK kit recall — AVID Medical, Inc.

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.

Official ID Z-1970-2026 · Official record ↗

Verify with the official sources:

CPSC — consumer products ↗ (aggregated here)
NHTSA — vehicles, car seats, tires ↗ (aggregated here; use NHTSA's VIN lookup to check a specific vehicle)
FDA — food, drugs, medical devices ↗ (aggregated here)
USDA FSIS — meat, poultry & egg products ↗ (not yet aggregated here)
Recalls.gov — the U.S. government’s all-agency portal ↗

Found something wrong or missing? Report a data error.

Compiled from official public-domain government data. Last checked July 24, 2026 at 3:00 AM UTC.