10,000 results
·
88ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
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