8,819 results
·
79ms
·
Sources: EU EUDAMED, US FDA
SHARP MEDICAL PRODUCTS, LLC Reactor and Sleeve REF 100-36-01 Size: Adult
FDA Enforcement
Class II
·Terminated·Sharp Medical Products·April 14, 2021
SHARP MEDICAL PRODUCTS, LLC Reactor and Sleeve REF 100-36-01 Size: Adult
FDA Recall
Terminated
·Sharp Medical Products·Product code GCJ·February 8, 2021
800-SERIES
FDA Adverse Event
Malfunction
·GETINGE IC PRODUCTION POLAND SP. Z O.O.·Product code FLE·June 2, 2020
5.1L BD NEXT GENERATION SHARPS COLLECTOR
FDA Adverse Event
Injury
·BD·Product code MMK·May 1, 2013
PLASTIC APPLICATOR OF REPLENS VAGINAL MOISTURIZER
FDA Adverse Event
Injury
·LIL' DRUG STORE PRODUCTS, INC.·Product code NUC·September 27, 2015
BD SHARPS COLLECTOR
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code FMI·September 16, 2019
ESSURE
FDA Adverse Event
Injury
·BAYER PHARMA AG·Product code HHS·January 2, 2018
800-SERIES
FDA Adverse Event
Malfunction
·GETINGE IC PRODUCTION POLAND SP. Z O.O.·Product code FLE·June 2, 2020
800-SERIES
FDA Adverse Event
Malfunction
·GETINGE IC PRODUCTION POLAND SP. Z O.O.·Product code FLE·June 2, 2020
INTRASIGHT
FDA Adverse Event
Malfunction
·PHILIPS VOLCANO·Product code IYO·March 20, 2023
SHARPS COLL 17L YELLOW
FDA Adverse Event
Injury
·BECTON DICKINSON·Product code MMK·October 16, 2020
INTRASIGHT
FDA Adverse Event
Malfunction
·VOLCANO CORPORATION·Product code IYO·January 29, 2024
INTRASIGHT MOBILE
FDA Adverse Event
Malfunction
·PHILIPS VOLCANO·Product code IYO·September 9, 2022
BIVONA
FDA Adverse Event
Injury
·SMITHS MEDICAL ASD, INC.·Product code JOH·November 13, 2020
INTRASIGHT
FDA Adverse Event
Malfunction
·PHILIPS VOLCANO·Product code IYO·March 25, 2022
LOFRIC ORIGO
FDA Adverse Event
Injury
·WELLSPECT HEALTHCARE·Product code EZD·June 26, 2025
BARDIA COUDE OLIVE TIP URETHRAL FOLEY CATHETER
FDA Adverse Event
Malfunction
·C.R. BARD, INC. (COVINGTON) -1018233·Product code KOD·August 24, 2020
BD SHARPS COLL 19L YELLOW
FDA Adverse Event
Injury
·BECTON DICKINSON·Product code FMI·December 3, 2022
L.TAMPONSORGCOTTONPLASTICREG+SUPERNONDO30CT
FDA Adverse Event
Malfunction
·TAMBRANDS MANUFACTURING, INC·Product code HEB·March 10, 2021
MCKESSON
FDA Adverse Event
Other
·MEDEGEN MEDICAL PRODUCTS·Product code MMK·January 12, 2011