9 results
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18ms
·
Sources: EU EUDAMED, US FDA
BIOSPSY FORCEPS
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
TABLEPAD,TOSHIBA 2 PC,TFM
FDA UDI
ALIMED, INC.·00733657237566·
De Soutter Medical
FDA UDI
DE SOUTTER MEDICAL LIMITED·05051471122826·K-WIRE - DOUBLE TROCAR 0.7mm DIA x 150mm
PM14 SOFT AIR COMPRESSOR
FDA 510(k)
FDA Class 2
·Anesthesiology
GATIFLOXIN
FDA 510(k)
FDA Class 2
·Microbiology
INTERSTIM II
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·January 17, 2013
SYMBIQ
FDA Adverse Event
Malfunction
·HOSPIRA·Product code FPA·November 24, 2010
ASR ACETABULAR CUPS 54
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD.-8010379·Product code KWA·July 8, 2014
TRULIANT Knee System including TRULIANT Tibial Inserts, also labeled as the following: a. TRULIANT CR Tibial Inserts; b. TRULIANT CR Slope + Tibial Inserts; c. TRULIANT CR Slope ++ Tibial Inserts; d. TRULIANT CRC Tibial Inserts; e. TRULIANT PS Tibial Inserts; f. TRULIANT PSC Tibial Inserts. NOTE: Information reflects Exactech recall expansion initiated on 02/07/2022.
FDA Enforcement
Class II
·Ongoing·Exactech, Inc.·October 13, 2021