20 results · 32ms · Sources: EU EUDAMED, US FDA

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OsteoFlo HydroFiber

FDA 510(k)
FDA Class 2 ·Orthopedic

I.V. Catheter

FDA 510(k)
FDA Class 2 ·General Hospital

WRO 300 WATER PURIFICATION SYSTEM FOR HEMODIALYSIS

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

BD LUER-LOK SYRINGE STERILE, SINGLE USE

FDA Adverse Event
Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·March 4, 2019

BD POSIFLUSH¿ XS PRE-FILLED FLUSH SYRINGE NACL 0.9%

FDA Adverse Event
Injury ·BECTON, DICKINSON AND CO.·Product code NGT·March 4, 2019

9616657-2019-00155

FDA Adverse Event
Injury ·March 20, 2019

BD POSIFLUSH¿ XS PRE-FILLED FLUSH SYRINGE NACL 0.9%

FDA Adverse Event
Malfunction ·BECTON, DICKINSON AND CO.·Product code NGT·August 15, 2019

BD POSIFLUSH XS PRE-FILLED FLUSH SYRINGE NACL

FDA Adverse Event
Malfunction ·BECTON, DICKINSON AND CO.·Product code FMF·February 6, 2019

ARTICULEZE M HEAD 36MM +12

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS INC US·Product code JDI·November 11, 2014

HOMECHOICE

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·September 10, 2011

ARGON MEDICAL DEVICES

FDA Adverse Event
Malfunction ·ARGON MEDICAL DEVICES·Product code LJS·July 17, 2013

BD POSIFLUSH¿ XS PRE-FILLED FLUSH SYRINGE

FDA Adverse Event
Injury ·BECTON, DICKINSON AND CO.·Product code NGT·February 5, 2019

BD POSIFLUSH¿ XS PRE-FILLED FLUSH SYRINGE

FDA Adverse Event
Injury ·BECTON, DICKINSON AND CO.·Product code FMF·February 8, 2019

BD POSIFLUSH¿ XS PRE-FILLED FLUSH SYRINGE

FDA Adverse Event
Injury ·BECTON, DICKINSON AND CO.·Product code NGT·February 6, 2019

BD POSIFLUSH¿ XS PRE-FILLED FLUSH SYRINGE NACL

FDA Adverse Event
Injury ·BECTON, DICKINSON AND CO.·Product code NGT·April 15, 2019

BD POSIFLUSH¿ XS PRE-FILLED FLUSH SYRINGE

FDA Adverse Event
Injury ·BECTON, DICKINSON AND CO.·Product code FMF·February 11, 2019

BD POSIFLUSH¿ XS PRE-FILLED FLUSH SYRINGE

FDA Adverse Event
Death ·BECTON, DICKINSON AND CO.·Product code NGT·January 28, 2019

BD POSIFLUSH¿ XS PRE-FILLED FLUSH SYRINGE NACL 0.9%

FDA Adverse Event
Malfunction ·BECTON, DICKINSON AND CO.·Product code NGT·March 21, 2019

BD POSIFLUSH XS PRE-FILLED FLUSH SYRINGE

FDA Adverse Event
Injury ·BECTON, DICKINSON AND CO.·Product code FMF·March 20, 2019

Model Number L111, ESSENTIO DR SL MRI Pacemaker

FDA Enforcement
Class I ·Ongoing·Boston Scientific Corporation·October 22, 2025