8 results
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30ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 13, 2014
IAB: 8 FR - 40 CC
FDA Adverse Event
Injury
·ARROW INTL., INC.·Product code DSP·October 8, 2010
ENDOCARE, CRYOCARE CRYOPROBE 3.8MM LONG
FDA Adverse Event
Malfunction
·HEALTHTRONICS, INC.·Product code GEH·December 12, 2012
BINAXNOW COVID-19 AG SELF TEST 4CT
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QKP·October 28, 2024
BINAXNOW COVID-19 AG SELF TEST 4CT
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QKP·August 5, 2024
BINAXNOW COVID-19 AG SELF TEST 4CT
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QKP·October 21, 2024
BINAXNOW COVID-19 AG SELF TEST 4CT
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QKP·October 28, 2024
BINAXNOW COVID-19 AG SELF TEST 4CT
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QKP·October 21, 2024