836 results
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20ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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P200TE (A10700)
FDA 510(k)
FDA Class 2
·Ophthalmic
BD BBL™ Sensi-Disc™ Cefpodoxime 10 µg
FDA UDI
BECTON, DICKINSON AND COMPANY·00382902316732·BD BBL™ Sensi-Disc™ Cefpodoxime 10 µg
REFOBACIN -PALACOS G
FDA 510(k)
FDA Class 2
·Orthopedic
MAGNIFUSE BONE GRAFT, MAGIFUSE II BONE GRAFT
FDA 510(k)
FDA Class 2
·Orthopedic
BD BBL Sensi Disc Cefpodoxime - 10 ug, used for semi-quantitative in vitro susceptibility testing. Catalog Number 231673 and 231674¿
FDA Enforcement
Class II
·Ongoing·Becton Dickinson & Co.·February 14, 2024
MECHANICAL (MANUAL) WHEELCHAIR
FDA Adverse Event
Malfunction
·INVACARE FLORIDA OPERATIONS·Product code IOR·November 6, 2014
UNKNOWN DEPUY ASR FEMORAL HEAD
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KWA·September 1, 2011
URETEX SUPPORT PP KIT X1
FDA Adverse Event
Injury
·SOFRADIM PRODUCTION·Product code OTN·July 12, 2013
BD BBL Sensi Disc Cefpodoxime - 10 ug, used for semi-quantitative in vitro susceptibility testing. Catalog Number 231673 and 231674
FDA Recall
Open, Classified
·Becton Dickinson & Co.·Product code JTN·January 8, 2024
IMP,TSV,4.1,11.5,MTX,MG
FDA Adverse Event
Injury
·ZIMMER DENTAL·Product code DZE·July 28, 2023
BD VACUTAINER® K2 EDTA (K2E) 3.6MG BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO (FRANKLIN LAKES)·Product code GIM·May 26, 2026
BD VACUTAINER® K2 EDTA (K2E) 3.6MG BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO (FRANKLIN LAKES)·Product code GIM·May 1, 2026
BD VACUTAINER® K2 EDTA (K2E) 5.4MG BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO (FRANKLIN LAKES)·Product code GIM·April 28, 2026
BD VACUTAINER® K2 EDTA (K2E) 5.4MG BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO (FRANKLIN LAKES)·Product code GIM·March 11, 2026
BD VACUTAINER® K2 EDTA (K2E) 3.6MG BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO (FRANKLIN LAKES)·Product code GIM·May 12, 2026
BD VACUTAINER® K2 EDTA (K2E) 5.4MG BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO (FRANKLIN LAKES)·Product code GIM·May 15, 2026
BD VACUTAINER® K2 EDTA (K2E) 10.8MG BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO (FRANKLIN LAKES)·Product code GIM·February 5, 2026
BD VACUTAINER® K2 EDTA (K2E) 5.4MG BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO (FRANKLIN LAKES)·Product code GIM·May 14, 2026
BD VACUTAINER® K2 EDTA (K2E) 10.8MG BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO (FRANKLIN LAKES)·Product code GIM·February 6, 2026
BD VACUTAINER® K2 EDTA (K2E) 10.8MG BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO (FRANKLIN LAKES)·Product code GIM·May 12, 2026