16 results
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48ms
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Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
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30 ML BD LUER-LOK¿ TIP SYRINGE
FDA Adverse Event
Malfunction
·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code FMF·August 31, 2022
ZIP CLOSURE WITH POUCH
FDA Adverse Event
Malfunction
·MEDICAL ACTION INDUSTRIES, INC.·Product code LIO·January 4, 2012
ZIP CLOSURE WITH POUCH
FDA Adverse Event
Malfunction
·MEDICAL ACTION INDUSTRIES, INC.·Product code NNI·September 21, 2011
SYNCHROMED II
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LKK·April 6, 2016
PALINDROME
FDA Adverse Event
Malfunction
·COVIDIEN MFG SOLUTIONS S.A.·Product code MSD·July 6, 2022
SURESCAN
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·April 27, 2016
DERMABOND ADVANCED 0.7ML - 12EA
FDA Adverse Event
Malfunction
·ETHICON INC.·Product code MPN·September 22, 2022
EVIS LUCERA COLONOVIDEOSCOPE
FDA Adverse Event
Malfunction
·AIZU OLYMPUS CO., LTD.·Product code FDF·November 18, 2022
PLUM A+ DRIVER ED 2
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FRN·September 6, 2013
SYNCHROMED II
FDA Adverse Event
Malfunction
·MDT PUERTO RICO OPERATIONS CO·Product code LKK·October 7, 2015
URINE COLLECTION
FDA Adverse Event
Malfunction
·C.R. BARD, INC. (COVINGTON) -1018233·Product code KNX·August 9, 2022
UNKNOWN SILICONE TEMP-SENSING CATHETER
FDA Adverse Event
Malfunction
·C.R. BARD, INC. (COVINGTON) -1018233·Product code EZL·August 12, 2022
UNKNOWN FOLEY CATHETER
FDA Adverse Event
Malfunction
·C.R. BARD, INC. (COVINGTON) -1018233·Product code EZC·August 10, 2022
ALL SILICONE CATHETER
FDA Adverse Event
Malfunction
·C.R. BARD, INC. (COVINGTON) -1018233·Product code EZL·August 10, 2022
ALL SILICONE CATHETER
FDA Adverse Event
Malfunction
·C.R. BARD, INC. (COVINGTON) -1018233·Product code EZL·August 10, 2022
JOEY PUMP SET
FDA Adverse Event
Malfunction
·COVIDIEN·Product code LZH·September 25, 2017