10,000 results · 88ms · 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

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

THERMACOOL

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

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

HANDSWITCH PENCIL W/ HOLSTER

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

NEOPUFF INFANT RESUSCITATOR

FDA Adverse Event
Malfunction ·FISHER & PAYKEL HEALTHCARE, LTD.·Product code BTM·March 3, 2008

INTELLIVUE MX40 WLAN

FDA Adverse Event
Malfunction ·PHILIPS MEDICAL SYSTEMS HSG·Product code MHX·June 16, 2022

N95 FACE MASKS

FDA Adverse Event
Malfunction ·HSM MED SUPPLY LLC·Product code QKR·September 10, 2021

DIGITRAK XT

FDA Adverse Event
Malfunction ·PHILIPS MEDICAL SYSTEMS HSG·Product code MWJ·February 21, 2023

DIGITRAK XT

FDA Adverse Event
Malfunction ·PHILIPS MEDICAL SYSTEMS HSG·Product code MWJ·February 28, 2023

DIGITRAK XT

FDA Adverse Event
Malfunction ·PHILIPS MEDICAL SYSTEMS HSG·Product code MWJ·December 1, 2022

LRG. HUDSON TO 1/4 SQ. ADAPTER

FDA Adverse Event
Malfunction ·ORTHOPEDIATRICS, CORP·Product code NKB·September 10, 2021

LIGASURE

FDA Adverse Event
Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·April 3, 2017