19 results
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19ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
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8000229
FDA Adverse Event
Malfunction
·LASER PERIPHERALS, LLC·Product code GEX·August 7, 2025
8000229
FDA Adverse Event
Malfunction
·LASER PERIPHERALS, LLC·Product code GEX·August 7, 2025
8000229
FDA Adverse Event
Malfunction
·LASER PERIPHERALS, LLC·Product code GEX·August 7, 2025
8000229
FDA Adverse Event
Malfunction
·LASER PERIPHERALS, LLC·Product code GEX·August 7, 2025
8000229
FDA Adverse Event
Malfunction
·LASER PERIPHERALS, LLC·Product code GEX·January 24, 2023
8000229
FDA Adverse Event
Malfunction
·LASER PERIPHERALS, LLC·Product code GEX·June 16, 2023
8000229
FDA Adverse Event
Malfunction
·LASER PERIPHERALS, LLC·Product code GEX·May 7, 2025
LUMIRADX SARS-COV-2 AG TEST STRIP KIT
FDA Adverse Event
Malfunction
·LUMIRADX UK LTD.·Product code QKP·February 25, 2021
LUMIRADX SARS-COV-2 AG TEST STRIP KIT
FDA Adverse Event
Malfunction
·LUMIRADX UK LTD.·Product code QKP·February 25, 2021
LUMIRADX SARS-COV-2 AG TEST STRIP KIT
FDA Adverse Event
Malfunction
·LUMIRADX UK LTD.·Product code QKP·February 25, 2021
LUMIRADX SARS-COV-2 AG TEST STRIP KIT
FDA Adverse Event
Malfunction
·LUMIRADX UK LTD.·Product code QKP·February 25, 2021
LUMIRADX SARS-COV-2 AG TEST STRIP KIT
FDA Adverse Event
Malfunction
·LUMIRADX UK LTD.·Product code QKP·February 25, 2021
LUMIRADX SARS-COV-2 AG TEST STRIP KIT
FDA Adverse Event
Malfunction
·LUMIRADX UK LTD.·Product code QKP·February 25, 2021
LUMIRADX SARS-COV-2 AG TEST STRIP KIT
FDA Adverse Event
Malfunction
·LUMIRADX UK LTD.·Product code QKP·February 25, 2021
LUMIRADX SARS-COV-2 AG TEST STRIP KIT
FDA Adverse Event
Malfunction
·LUMIRADX UK LTD.·Product code QKP·February 25, 2021
LUMIRADX SARS-COV-2 AG TEST STRIP KIT
FDA Adverse Event
Malfunction
·LUMIRADX UK LTD.·Product code QKP·February 25, 2021
LUMIRADX SARS-COV-2 AG TEST STRIP KIT
FDA Adverse Event
Malfunction
·LUMIRADX UK LTD.·Product code QKP·February 25, 2021
TREATMENT RECLINER
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code FRK·February 3, 2011
8010042-2008-00010
FDA Adverse Event
Malfunction
·Product code CBK·January 25, 2008