Namic Angiographic Manifold: recall status

⚠ Recalls found. Namic Angiographic Manifold is named in 3 official recalls in our current data:

FDA Class I recall Z-2138-2026 — Medline has identified the presence of particulate within the fluid path of the Manifolds.
FDA Class I recall Z-2139-2026 — Medline has identified the presence of particulate within the fluid path of the Manifolds.
FDA Class I recall Z-2140-2026 — Medline has identified the presence of particulate within the fluid path of the Manifolds.

Recalls naming this model

FDA Class I · Medical device · May 20, 2026

Medline has identified the presence of particulate within the fluid path of the Manifolds.

Official ID Z-2138-2026 · Official record ↗

FDA Class I · Medical device · May 20, 2026

Medline has identified the presence of particulate within the fluid path of the Manifolds.

Official ID Z-2139-2026 · Official record ↗

FDA Class I · Medical device · May 20, 2026

Medline has identified the presence of particulate within the fluid path of the Manifolds.

Official ID Z-2140-2026 · 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.