Fresh Recalls

Percutaneous Insertion Kit (PIK): recall status

⚠ Recalls found. Percutaneous Insertion Kit (PIK) is named in 3 official recalls in our current data:

Brand
Maquet Cardiopulmonary

Recalls naming this model

FDA Class II · Medical device · September 23, 2026

Percutaneous Insertion Kit (PIK) recall — Maquet Cardiopulmonary Gmbh

The packaging may not consistently maintain sterile barrier integrity.

Company / brand: Maquet Cardiopulmonary recalls

Affected product: Percutaneous Insertion Kit (PIK) recall status

Official ID Z-3144-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

Percutaneous Insertion Kit (PIK) recall — Maquet Cardiopulmonary Gmbh

The packaging may not consistently maintain sterile barrier integrity.

Company / brand: Maquet Cardiopulmonary recalls

Affected product: Percutaneous Insertion Kit (PIK) recall status

Official ID Z-3145-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

Percutaneous Insertion Kit (PIK) recall — Maquet Cardiopulmonary Gmbh

The packaging may not consistently maintain sterile barrier integrity.

Company / brand: Maquet Cardiopulmonary recalls

Affected product: Percutaneous Insertion Kit (PIK) recall status

Official ID Z-3146-2026 · Official record ↗

See all Maquet Cardiopulmonary recalls →

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