8 results
·
23ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
BD CD81 APC-H7 (JS-81) ASR
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND COMPANY, BD BIOSCIENCES·Product code MVU·July 14, 2020
SYNCHRON (R) SYSTEMS CREATININE REAGENT
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code CGX·July 2, 2011
PROULTRA ENDO TIPS
FDA Adverse Event
Malfunction
·DENTSPLY MAILLEFER·Product code ELC·June 8, 2006
DURASTAR STRETCHER
FDA Adverse Event
Malfunction
·HILL-ROM INC.·Product code FPO·November 23, 2010
ENDOTAK RELIANCE
FDA Adverse Event
Malfunction
·CPI - DEL CARIBE·Product code NVY·January 11, 2013
NON AC-POWERED PATIENT LIFT
FDA Adverse Event
Malfunction
·INVACARE REHABILITATION EQUIP·Product code FSA·July 2, 2014
SMITHS MEDICAL PORTEX TRACHEOSTOMY TUBE BLUE LINE ULTRA
FDA Adverse Event
Malfunction
·SMITHS MEDICAL ASD, INC.·Product code JOH·November 18, 2019
PORTEX BLUE LINA ULTRA SUCTIONAID TRACH TUBE
FDA Adverse Event
Malfunction
·SMITHS MEDICAL INTERNATIONAL, LTD.·Product code BTO·July 5, 2022