PENCAN N/A 4454820

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional report with the FDA on 2017-12-07 for PENCAN N/A 4454820 manufactured by B. Braun Melsungen Ag.

Event Text Entries

[94126421] (b)(4). No sample has been returned for investigation. The batch record could not be reviewed since the lot number is not known. Without the actual sample or lot number, a thorough investigation can not be performed. All available information has been forwarded to the actual manufacturer.
Patient Sequence No: 1, Text Type: N, H10


[94126422] As reported by the user facility ((b)(4)): broken cannula. About 3 cm left inside of patient, which required an extra operation to remove.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9610825-2017-00240
MDR Report Key7095888
Report SourceFOREIGN,HEALTH PROFESSIONAL
Date Received2017-12-07
Date of Report2017-12-07
Date Facility Aware2017-12-07
Report Date2017-12-07
Date Reported to FDA2017-12-07
Date Reported to Mfgr2017-12-07
Date Mfgr Received2017-11-09
Date Added to Maude2017-12-07
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMR. JONATHAN SEVERINO
Manufacturer Street861 MARCON BLVD.
Manufacturer CityALLENTOWN 18109
Manufacturer CountryUS
Manufacturer Postal18109
Manufacturer Phone4842408332
Manufacturer G1B. BRAUN MELSUNGEN AG
Manufacturer StreetCARL-BRAUN-STR. 1
Manufacturer CityMELSUNGEN, 34212
Manufacturer CountryGM
Manufacturer Postal Code34212
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NamePENCAN
Generic NameSPINAL NEEDLE
Product CodeMIA
Date Received2017-12-07
Model NumberN/A
Catalog Number4454820
Lot NumberUNKNOWN
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerB. BRAUN MELSUNGEN AG
Manufacturer AddressCARL-BRAUN-STR. 1 MELSUNGEN, HESSEN 34212 GM 34212


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2017-12-07

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.