Halyard: recall status

⚠ Recalls found. Halyard is named in 4 official recalls in our current data:

FDA Class II recall Z-2407-2026 — Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
FDA Class II recall Z-2408-2026 — Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
FDA Class II recall Z-2409-2026 — Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
And 1 more listed below.

Recalls naming this model

FDA Class II · Medical device · June 17, 2026

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

Company / brand: AVID Medical

Affected product: Halyard

Official ID Z-2407-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

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

Company / brand: AVID Medical

Affected product: Halyard

Official ID Z-2408-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

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

Company / brand: AVID Medical

Affected product: Halyard

Official ID Z-2409-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

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

Company / brand: AVID Medical

Affected product: Halyard

Official ID Z-2410-2026 · Official record ↗

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Compiled from connected official public-domain government data. Sources last checked September 7, 2026 at 6:00 AM UTC.