Medical device recalls

Datascope Corp/MAQUET recalls Datascope Corp/MAQUET — Intra-Aortic Balloon Pumps

Recall date
February 8, 2018
Source
U.S. Food & Drug Administration (FDA) — recall announcement
Brand / firm
Datascope Corp/MAQUET, Datascope Corp/MAQUET

Why it was recalled

Potential electrical test failure code — Device & Drug Safety

What was recalled

Intra-Aortic Balloon Pumps

Read the official recall notice →

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