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 ...
Healio

Intra-aortic balloon pumps voluntarily recalled after patient death

Please provide your email address to receive an email when new articles are posted on . The FDA issued a safety alert announcing that Datascope Corp. issued a voluntary field correction for ...
Healio

Hybrid intra-aortic balloon pump recalled

Please provide your email address to receive an email when new articles are posted on . The FDA announced that Maquet Datascope Corp. has recalled a hybrid intra-aortic balloon pump due to a design ...