85 results · 45ms · Sources: EU EUDAMED, US FDA

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5 ML EXACTA MED ORAL LIQUID DISPENSER

FDA Adverse Event
Malfunction ·BAXA CORP·Product code LHI·April 30, 2010

EXACTA-MIX 2400, MAIN MODULE

FDA Adverse Event
Malfunction ·BAXA CORPORATION·Product code LHI·June 11, 2010

EXACTA-MIX EMPTY EVA CONTAINER

FDA Adverse Event
Malfunction ·BAXA CORPORATION·Product code LHI·May 12, 2010

EXACTA-MIX 2400

FDA Adverse Event
Other ·BAXA CORP.·Product code NEP·May 6, 2010

TPN PC PLUS

FDA Adverse Event
Injury ·BAXA CORP.·Product code LNX·October 28, 2003

EXACTA-MIX EMPTY EVA CONTAINER

FDA Adverse Event
Malfunction ·BAXA CORP.·Product code KPE·April 2, 2010

EXACTA-MED ORAL DISPENSERS 0.5ML/1ML/3ML/5ML

FDA Adverse Event
Malfunction ·BAXA CORPORATION·Product code KYX·February 7, 2007

TWO-FER NEEDLES

FDA Adverse Event
Malfunction ·BAXA CORP.·Product code LHI·August 17, 2009

EXACTA-MIX EMPTY EVA CONTAINER

FDA Adverse Event
Malfunction ·BAXA CORP.·Product code KPE·January 14, 2010

EXACTA-MIX, EVA CONTAINER, 3-LITER CAPACITY

FDA Adverse Event
Malfunction ·BAXA CORP.·Product code KPE·September 1, 2011

COAGUCHEK® XS SYSTEM

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code GJS·April 12, 2010

COAGUCHEK® XS SYSTEM

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code GJS·April 27, 2010

COAGUCHEK® XS SYSTEM

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code GJS·April 29, 2010

EM2400 VALVE SET

FDA Adverse Event
Malfunction ·BAXA CORP.·Product code LHI·February 26, 2009

MICROFUSE RAPID RATE INFUSER

FDA Adverse Event
Malfunction ·BAXA CORP.·Product code FRN·September 28, 2006

IVT DISPOSABLE

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - AIBONITO·Product code KPE·October 19, 2011

SIGMA

FDA Adverse Event
Malfunction ·SIGMA INTERNATIONAL·Product code FRN·November 10, 2004

SMARTSITE EXTENSION SET

FDA Adverse Event
Malfunction ·CAREFUSION·Product code FPA·November 12, 2015

EXACTAMIX® 2400 COMPOUNDER

FDA Adverse Event
Injury ·BAXA CORPORATION·Product code NEP·March 26, 2012

EXACTAMIX

FDA Adverse Event
Malfunction ·BAXA CORPORATION·Product code NEP·February 9, 2012