10,000 results · 117ms · Sources: EU EUDAMED, US FDA

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OFF SET DOUBLE CLAMP BAR

FDA Adverse Event
Malfunction ·ZIMMER ORTHO SURGICAL PRODUCTS·Product code HSQ·March 5, 2002

ZIMMER

FDA Adverse Event
Malfunction ·ZIMMER, INC.·Product code HSQ·March 19, 2001

OFFSET DOUBLE CLAMP BAR

FDA Adverse Event
Injury ·ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS·Product code HSQ·August 23, 2005

PANEL CLAMP UPPER AND LOWER

FDA Adverse Event
Malfunction ·ZIMMER PATIENT CARE·Product code HSQ·April 6, 2001

ZIMMER TRAPEZE

FDA Adverse Event
Malfunction ·ZIMMER PATIENT CARE·Product code HSQ·May 23, 2001

ZIMMER CLAMP ASSEMBLY

FDA Adverse Event
Other ·ZIMMER PATIENT CARE·Product code HSQ·April 24, 2001

THERMACOOL

FDA Adverse Event
Malfunction ·THERMAGE·Product code GEI·December 22, 2005

AMBULIFT BSQ

FDA Adverse Event
Other ·ARJO LTD.·Product code FSA·July 26, 2000

AMBULIFT BSQ

FDA Adverse Event
Malfunction ·ARJO LTD.·Product code FSA·October 30, 2001

AMBULIFT BSQ

FDA Adverse Event
Malfunction ·ARJO LTD.·Product code FSA·November 19, 2001

AMBULIFT BSQ

FDA Adverse Event
Malfunction ·ARJO, LTD.·Product code FSA·September 21, 2001

AMBULIFT BSQ

FDA Adverse Event
Malfunction ·ARJO HOSPITAL EQUIPMENT AB·Product code FSA·July 22, 2010

NEEDLE CLIPPING DEVICE SAFE CLIP

FDA Adverse Event
Malfunction ·HDQ PARSIPPANY·Product code FMI·February 23, 2024

UNKNOWN

FDA Adverse Event
Malfunction ·HDQ PARSIPPANY·Product code MMK·February 5, 2024

ARJO AMBULIFT BSQ

FDA Adverse Event
Other ·ARJO MANUFACTURING CO.·Product code FSA·August 8, 1996

ARJO AMBULIFT BSQ

FDA Adverse Event
Other ·ARJO MANUFACTURING CO.·Product code FSA·January 3, 1997

CONMED ELECTROSURGICAL DISPERSIVE ELECTRODE

FDA Adverse Event
Injury ·CONMED CORPORATION·Product code GEI·August 25, 1997

HOTDOG UNDER BODY WARMING MATTRESS 127 CM ( 50")

FDA Adverse Event
Injury ·AUGUSTINE TEMPERATURE MANAGEMENT·Product code DWJ·January 22, 2025

MALEM ULTIMATE BEDWETTING ALARM

FDA Adverse Event
Injury ·MALEM MEDICAL LTD.·Product code KPN·May 21, 2019

HANDSWITCH PENCIL W/ HOLSTER

FDA Adverse Event
Malfunction ·COVIDIEN LP (VALLEYLAB)·Product code GEI·December 20, 2007