7 results
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17ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
OASIS DRY SUCTION WATER SEAL CHESTDRAIN
FDA Adverse Event
Malfunction
·ATRIUM MEDICAL CORPORATION·Product code CAC·November 7, 2013
ENDOPATH** XCEL* BLADELESS TROCAR
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code GCJ·July 10, 2013
HEARTSTART HOME
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code NSA·March 1, 2013
ENDOWRIST
FDA Adverse Event
Malfunction
·INTUITIVE SURGICAL, INC·Product code NAY·August 10, 2020
ALINITY M RESP-4-PLEX AMPLIFICATION REAGENT KIT
FDA Adverse Event
Malfunction
·ABBOTT MOLECULAR, INC.·Product code QJR·October 19, 2022
ALINITY M RESP-4-PLEX AMPLIFICATION REAGENT KIT
FDA Adverse Event
Malfunction
·ABBOTT MOLECULAR, INC.·Product code QJR·October 28, 2022
ALINITY M RESP-4-PLEX AMPLIFICATION REAGENT KIT
FDA Adverse Event
Malfunction
·ABBOTT MOLECULAR, INC.·Product code QJR·October 28, 2022