Medscape

FDA Expands Datascope IABP Field Correction to Class I Recall

SILVER SPRING, MD —The US Food and Drug Administration has expanded the June 2017 onsite field correction issued for Datascope/Maquet intra-aortic balloon pumps (IABPs) to a class I recall, the agency ...
Medscape

Field Correction for Datascope Intra-aortic Balloon Pumps

SILVER SPRING, MD — Datascope Corp/Maquet has initiated a worldwide "field correction" of certain intra-aortic balloon pump (IABP) systems to address potential electrical test failures, a MedWatch ...
TCTMD

Recall Underway for Certain IABPs Due to Potential Electrical Test Failure

Datascope/Maquet have initiated a worldwide recall of certain intra-aortic balloon pump (IABP) systems to address potential electrical test failures. The action involves CS100, CS100i, and CS300 IABPs ...
TCTMD

Maquet Recalls Intra-Aortic Balloon Pumps Due to Potential Failure of Power Supply

— Datascope Corp./Maquet initiated a voluntary worldwide field correction of some of its intra-aortic balloon pumps (IABPs) due to a potential mechanical failure of the fan assembly associated with ...