127 results
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31ms
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Sources: EU EUDAMED, US FDA
Filters
Status: Injury
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SKIN STAPLER 35W
FDA Adverse Event
Injury
·TELEFLEX LLC·Product code QQS·December 23, 2025
MICRO PUNCTURE KIT
FDA Adverse Event
Injury
·TELEFLEX LLC·Product code DYB·August 1, 2024
SKIN STAPLER 35W
FDA Adverse Event
Injury
·TELEFLEX LLC·Product code QQS·August 9, 2024
SKIN STAPLER 35W
FDA Adverse Event
Injury
·TELEFLEX LLC·Product code QQS·August 9, 2024
SKIN STAPLER 35W
FDA Adverse Event
Injury
·TELEFLEX LLC·Product code QQS·August 9, 2024
SKIN STAPLER 35W
FDA Adverse Event
Injury
·TELEFLEX LLC·Product code QQS·August 9, 2024
TELEFLEX NITINOL GUIDEWIRE
FDA Adverse Event
Injury
·TELEFLEX LLC (NADC)·Product code DQX·August 28, 2023
O'REILLY ESOPHAGEAL RETRACTOR
FDA Adverse Event
Injury
·TELEFLEX LLC (NADC)·Product code KAL·December 5, 2022
KMEDIC LAMBOTTE OSTEOTOME
FDA Adverse Event
Injury
·TELEFLEX LLC (NADC)·Product code GFI·March 30, 2026
UROLIFT
FDA Adverse Event
Injury
·TELEFLEX, INC. / TELEFLEX LLC (NADC)·Product code PEW·May 23, 2024
ARROWG+ARD
FDA Adverse Event
Injury
·TELEFLEX / TELEFLEX LLC (NADC 2)·Product code FOZ·July 19, 2023
KIT CATH MTLUM PRES INJ CVC LF
FDA Adverse Event
Injury
·TELEFLEX LLC / / ARROW INTERNATIONAL LLC·Product code DQY·April 24, 2020
ARROW RADIAL ARTERIAL CATHETERIZATION SET
FDA Adverse Event
Injury
·ARROW INTERNATIONAL, LLC / TELEFLEX LLC (NADC)·Product code DQX·January 22, 2026
MANTA CLOSURE DEVICE 18FR UNK
FDA Adverse Event
Injury
·TELEFLEX MEDICAL LLC·Product code MGB·December 30, 2025
SHERIDAN/CF ENDOTRACHEAL TUBE
FDA Adverse Event
Injury
·TELEFLEX MEDICAL LLC.·Product code BTR·November 4, 2025
SHERIDAN/CF ENDOTRACHEAL TUBE
FDA Adverse Event
Injury
·TELEFLEX MEDICAL LLC.·Product code BTR·November 4, 2025
UROLIFT SYSTEM
FDA Adverse Event
Injury
·TELEFLEX MEDICAL LLC.·Product code PEW·November 24, 2025
UROLIFT
FDA Adverse Event
Injury
·TELEFLEX MEDICAL LLC·Product code PEW·July 7, 2025
HEM O LOK SURGICAL CLIPS
FDA Adverse Event
Injury
·TELEFLEX MEDICAL LLC.·Product code FZP·April 16, 2025
ARROW FLEXBLOCK CONTINUOUS PERIPHERAL NERVE BLOCK TRAY - FB-19609-K
FDA Adverse Event
Injury
·TELEFLEX MEDICAL LLC·Product code CAZ·April 9, 2026