Fresh Recalls

Abiomed REF: recall status

⚠ Recalls found. Abiomed REF is named in 3 official recalls in our current data:

Brand
Oscor

Recalls naming this model

FDA Class I · Medical device · July 22, 2026

Abiomed REF recall — Oscor Inc.

Due to manufacturing issues, there is a potential for the 14Fr and 23Fr introducer sheaths to leak from the sidearm, under the sheath cap, and along the hub score lines in the hub …

Company / brand: Oscor recalls

Affected product: Abiomed REF recall status

Official ID Z-2678-2026 · Official record ↗

FDA Class I · Medical device · July 22, 2026

Abiomed REF recall — Oscor Inc.

Due to manufacturing issues, there is a potential for the 14Fr and 23Fr introducer sheaths to leak from the sidearm, under the sheath cap, and along the hub score lines in the hub …

Company / brand: Oscor recalls

Affected product: Abiomed REF recall status

Official ID Z-2679-2026 · Official record ↗

FDA Class I · Medical device · July 22, 2026

Abiomed REF recall — Oscor Inc.

Due to manufacturing issues, there is a potential for the 14Fr and 23Fr introducer sheaths to leak from the sidearm, under the sheath cap, and along the hub score lines in the hub …

Company / brand: Oscor recalls

Affected product: Abiomed REF recall status

Official ID Z-2680-2026 · Official record ↗

See all Oscor recalls →

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Compiled from connected official public-domain government data. Sources last checked October 22, 2026 at 6:00 PM UTC.