8 results
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37ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
PORTEX
FDA Adverse Event
Malfunction
·SMITHS MEDICAL INTERNATIONAL, LTD.·Product code BTO·August 7, 2020
PORTEX BLUE LINE ULTRA SUCTIONAID TUBE WITH SOFT-SEAL CUFF AND INNER CANNULAE
FDA Adverse Event
Malfunction
·SMITHS MEDICAL ASD, INC.·Product code JOH·June 26, 2019
PORTEX BLUE LINE ULTRA SUCTIONAID TUBE WITH SOFT-SEAL CUFF AND INNER CANNULAE
FDA Adverse Event
Malfunction
·SMITHS MEDICAL ASD, INC.·Product code JOH·June 26, 2019
PORTEX
FDA Adverse Event
Malfunction
·SMITHS MEDICAL INTERNATIONAL, LTD.·Product code BTO·August 29, 2020
BLUE LINE ULTRA
FDA Adverse Event
Malfunction
·SMITHS MEDICAL ASD, INC·Product code JOH·July 18, 2019
CENTURION VISION SYSTEM
FDA Adverse Event
Malfunction
·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·April 29, 2014
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Injury
·MEDTRONIC MINIMED·Product code OYC·December 12, 2012
ACCENT DR
FDA Adverse Event
Injury
·ST. JUDE MEDICAL, INC.(CRM-SYLMAR)·Product code LWP·June 25, 2015