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🇺🇸·Jul 22Regulatory

Device recall: Abiomed REF: 0052-3025, Introducer Kit for Impella Hemostatic Peel Away Introducer System with Infusion Sideport, 14F 13cm and 25cm. heart pump and accessories.

Official structured record identifier: 99102.

Publisher

o
openFDA Device Recalls

USA

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Publisher
openFDA Device Recalls
Region
USA
Scope
Regulatory
Published
July 22, 2026
Language
EN

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Official structured record identifier: 99102.

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Source: openFDA Device Recalls

Scope: Regulatory

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Device recall: Abiomed REF: 0052-3025, Introducer Kit for Impella Hemostatic Peel Away Introducer System with Infusion Sideport, 14F 13cm and 25cm. heart pump and accessories. | Pharma Surge