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