BONE WAX 24X2.5G 1029754

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative report with the FDA on 2017-09-29 for BONE WAX 24X2.5G 1029754 manufactured by B.braun Surgical Sa.

Event Text Entries

[87873785] (b)(4). Manufacturing site evaluation: evaluation on-going.
Patient Sequence No: 1, Text Type: N, H10


[87873787] Country of complaint: usa. Bone wax seems to have melted and adhered to the clear part of the packaging.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3003639970-2017-00485
MDR Report Key6903911
Report SourceCOMPANY REPRESENTATIVE
Date Received2017-09-29
Date of Report2017-11-01
Date Facility Aware2017-09-19
Date Mfgr Received2017-09-07
Date Added to Maude2017-09-29
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMS. NICOLE BROYLES
Manufacturer Street615 LAMBERT POINTE DRIVE
Manufacturer CityHAZELWOOD MO 63042
Manufacturer CountryUS
Manufacturer Postal63042
Manufacturer Phone3145515988
Manufacturer G1AESCULAP AG
Manufacturer StreetPO BOX 40
Manufacturer CityTUTTLINGEN, 78501
Manufacturer CountryGM
Manufacturer Postal Code78501
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameBONE WAX 24X2.5G
Generic NameBONE WAX
Product CodeMTJ
Date Received2017-09-29
Returned To Mfg2017-09-25
Model Number1029754
Catalog Number1029754
Lot Number216443
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerB.BRAUN SURGICAL SA
Manufacturer Address121 CARRETERA DE TERRASSA RUBI, 08191 SP 08191


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2017-09-29

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