AllClear
PricingSign in
FDASeptember 20, 2018device

Cardiosave Hybrid IABP, Part Number 0998-00-0800-53

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

There is a potential for interruption and/or inability to start therapy to the patient prior to or during use of Cardiosave IABP for users who are at altitudes above 3200 Ft.

What to do

FDA enforcement status: Ongoing

Brands named

maquet datascope corp cardiac assist divisionmaquetmaquet datascope

UPCs

10607567108391099800080053

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

Own something like this?

AllClear screens your whole list against every CPSC, FDA, USDA and NHTSA recall — and tells you the day a new one names something you own.

Start free — 200 items, no card →