ENDOBON? XENOGRAFT GRANULES 0.5ML N/A ROX05

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor,foreign,health pr report with the FDA on 2018-01-09 for ENDOBON? XENOGRAFT GRANULES 0.5ML N/A ROX05 manufactured by Biomet France S.a.r.l..

Event Text Entries

[96750241] (b)(4). Concomitant medical products: full osseotite? Tapered implant 4 x 10 mm. (b)(6). Customer has indicated that the product will not be returned to zimmer biomet for investigation. The investigation is in process. Once the investigation has been completed, a follow-up mdr will be submitted.
Patient Sequence No: 1, Text Type: N, H10


[96750242] It was reported that after a sinus lift was performed and refilled with endobon, the surgeon noticed an infection. Three of the four implants placed failed. Attempts have been made and additional information on the reported event is unavailable.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3006946279-2018-00003
MDR Report Key7175318
Report SourceDISTRIBUTOR,FOREIGN,HEALTH PR
Date Received2018-01-09
Date of Report2019-01-24
Date Mfgr Received2019-01-24
Device Manufacturer Date2014-08-22
Date Added to Maude2018-01-09
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. H BATAILLE
Manufacturer StreetPLATEAU DE LAUTAGNE BP75
Manufacturer CityVALENCE IN 26903
Manufacturer CountryFR
Manufacturer Postal26903
Manufacturer Phone5745273773
Manufacturer G1BIOMET FRANCE S.A.R.L.
Manufacturer StreetPLATEAU DE LAUTAGNE BP75
Manufacturer CityVALENCE CEDEX 26903
Manufacturer CountryFR
Manufacturer Postal Code26903
Single Use3
Previous Use Code3
Removal Correction NumberN/A
Event Type3
Type of Report3

Device Details

Brand NameENDOBON? XENOGRAFT GRANULES 0.5ML
Generic NameBONE GRAFTING MATERIAL, SYNTHETIC
Product CodeLYC
Date Received2018-01-09
Model NumberN/A
Catalog NumberROX05
Lot NumberU0092202
ID Number(01) 03599870091258
Device Expiration Date2017-06-30
OperatorPHYSICIAN
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerBIOMET FRANCE S.A.R.L.
Manufacturer AddressPLATEAU DE LAUTAGNE BP75 VALENCE CEDEX 26903 FR 26903


Patients

Patient NumberTreatmentOutcomeDate
101. Hospitalization; 2. Required No Informationntervention 2018-01-09

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