9 results
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30ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
HFV PATIENT CIRCUIT
FDA Adverse Event
Malfunction
·BUNNELL·Product code LSZ·September 14, 2012
HFV PATIENT CIRCUIT
FDA Adverse Event
Malfunction
·BUNNELL·Product code LSZ·September 14, 2012
HFV PATIENT CIRCUIT
FDA Adverse Event
Malfunction
·BUNNELL·Product code LSZ·September 14, 2012
COBAS® EGFR MUTATION TEST V2 P150044
FDA Adverse Event
Malfunction
·ROCHE MOLECULAR SYSTEMS, INC. - BRANCHBURG·Product code OWD·April 1, 2026
COBAS® EGFR MUTATION TEST V2 P150044
FDA Adverse Event
Malfunction
·ROCHE MOLECULAR SYSTEMS, INC. - BRANCHBURG·Product code OWD·April 15, 2026
COBAS® EGFR MUTATION TEST V2 P150044
FDA Adverse Event
Malfunction
·ROCHE MOLECULAR SYSTEMS, INC. - BRANCHBURG·Product code OWD·March 27, 2025
ASR XLA STD SLEEVE 12/14 +5
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD. 8010379·Product code KWY·June 4, 2014
S-ROM M HEAD 36MM +0
FDA Adverse Event
Injury
·Product code JDI·November 29, 2012
PUMP MMT-522LNAL PRDGM INS CL EN ML
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code MDS·September 27, 2010