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NIMBUS II PLUS AMBULATORY INFUSION PUMP

FDA Adverse Event
Malfunction ·INFUTRONIX, LLC·Product code FRN·April 9, 2024

NIMBUS II PAINPRO AMBULATORY INFUSION PUMP

FDA Adverse Event
Malfunction ·INFUTRONIX, LLC·Product code FRN·April 11, 2024

NIMBUS II PAINPRO AMBULATORY INFUSION PUMP

FDA Adverse Event
Malfunction ·INFUTRONIX, LLC·Product code FRN·April 11, 2024

NIMBUS II PAINPRO AMBULATORY INFUSION PUMP

FDA Adverse Event
Malfunction ·INFUTRONIX, LLC·Product code FRN·April 11, 2024

NIMBUS II PAINPRO AMBULATORY INFUSION PUMP

FDA Adverse Event
Malfunction ·INFUTRONIX, LLC·Product code FRN·April 11, 2024

NIMBUS II PAINPRO AMBULATORY INFUSION PUMP

FDA Adverse Event
Malfunction ·INFUTRONIX, LLC·Product code FRN·April 11, 2024

NIMBUS II PLUS AMBULATORY INFUSION PUMP

FDA Adverse Event
Malfunction ·INFUTRONIX, LLC·Product code FRN·April 8, 2024

NIMBUS II PAINPRO AMBULATORY INFUSION PUMP

FDA Adverse Event
Malfunction ·INFUTRONIX, LLC·Product code FRN·April 11, 2024

NIMBUS II PAINPRO AMBULATORY INFUSION PUMP

FDA Adverse Event
Malfunction ·INFUTRONIX, LLC·Product code FRN·April 11, 2024

NIMBUS II PAINPRO AMBULATORY INFUSION PUMP

FDA Adverse Event
Malfunction ·INFUTRONIX, LLC·Product code FRN·April 11, 2024

The Fresenius APD Luer-Lock Adapter, Catalog number 050-95018, is designed to connect a peritoneal dialysis bag equipped with a luer-lock connector to a Fresenius Automated Peritoneal Dialysis (APD) cycler set that uses the Fresenius Safe-Lock¿ connector (e.g., Liberty¿ cycler, Newton IQO cycler).

FDA Enforcement
Class II ·Terminated·Fresenius Medical Care Holdings, Inc.·July 28, 2021

NIMBUS II PAINPRO AMBULATORY INFUSION PUMP

FDA Adverse Event
Malfunction ·INFUTRONIX, LLC·Product code FRN·April 11, 2024

NIMBUS II PAINPRO AMBULATORY INFUSION PUMP

FDA Adverse Event
Malfunction ·INFUTRONIX, LLC·Product code FRN·April 11, 2024

NIMBUS II PAINPRO AMBULATORY INFUSION PUMP

FDA Adverse Event
Malfunction ·INFUTRONIX, LLC·Product code FRN·April 11, 2024

NIMBUS II PAINPRO AMBULATORY INFUSION PUMP

FDA Adverse Event
Malfunction ·INFUTRONIX, LLC·Product code FRN·April 11, 2024

HYBRID GLENOID TRIAL PS 4MM LARGE

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code IQO·May 17, 2010

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FDA Adverse Event
Malfunction ·SMITH & NEPHEW RICHARD, INC.·Product code IQO·March 5, 2004

HYBRID GLENOID INSTRUMENT DRILL GUIDE ALIGNMENT PIN

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code IQO·June 19, 2012

VANGUARD UNV 5IN1 TIBIAL TRIAL 71/75X10

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code IQO·April 20, 2012

COMPREHENSIVE INSTRUMENTION HUMERAL TRIAL 44MM STANDARD - 36MM STANDARD

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code IQO·April 3, 2012