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Mikro-Cath Pressure Catheter

MILLAR INC. · Model 825-0101 · UDI-DI 00868924000205

DXO Prescription

510(k) clearances

2,406

Adverse events (21 deaths)

Recalls

Facilities

Description

The Millar Mikro-Cath Cardiovascular Catheter is fitted with an ultra-miniature pressure sensor near the distal end. The sensor is side mounted at the catheter tip. The proximal end terminates in a connector. The pressure sensor produces an electrical output signal which varies in direct proportion to the magnitude of sensed pressure or sound.

Recalls

Date	Firm	Reason
2021-05-26	Edwards Lifesciences, LLC	There is a potential that the pressure tubing may detach from the blood sampling system
2021-05-26	Edwards Lifesciences, LLC	There is a potential that the pressure tubing may detach from the blood sampling system
2021-05-26	Edwards Lifesciences, LLC	There is a potential that the pressure tubing may detach from the blood sampling system
2021-05-26	Edwards Lifesciences, LLC	There is a potential that the pressure tubing may detach from the blood sampling system
2021-05-26	Edwards Lifesciences, LLC	There is a potential that the pressure tubing may detach from the blood sampling system
2021-05-26	Edwards Lifesciences, LLC	There is a potential that the pressure tubing may detach from the blood sampling system
2021-05-26	Edwards Lifesciences, LLC	There is a potential that the pressure tubing may detach from the blood sampling system
2021-05-26	Edwards Lifesciences, LLC	There is a potential that the pressure tubing may detach from the blood sampling system
2015-11-13	Edwards Lifesciences, LLC	Edward Lifesciences is recalling Intravascular (IV) Administration Sets due to the requirement of an additional FDA submission to support commercialization (clearance) of the devic
2015-07-31	Edward Lifesciences, Llc	Flow restriction issues in a trifurcated IV set included in the pressure transducer kits. A restriction of the flow of IV fluid would result in either an inability to prime the sys

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.