COPIOS PERICARDIUM XENOGRAFT MEMBRANES

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2017-09-05 for COPIOS PERICARDIUM XENOGRAFT MEMBRANES manufactured by Tutogen Medical Gmbh.

Event Text Entries

[84805687] Method: rti/tmi will conduct a re-review of the product history record for copios pericardium membranes, packaging production records, environmental monitoring, distribution for related complaints associated to the lot. Results: pending; conclusion: pending; a follow-up med watch will be submitted.
Patient Sequence No: 1, Text Type: N, H10


[84805688] Rti surgical inc, (rti) and tutogen medical (b)(4) (tmi) a wholly owned subsidiary of (rti), received a complaint on 08/08/2017 which indicated that on (b)(6) 2016, a female patient underwent a sinus lift, with implantation of 5 copios xenograft particles (not distributed by rti us) and 2 copios pericardium membranes. It was reported that the biomaterial did not integrate and inflammation, infection and edema were noted. A second surgery is scheduled for (b)(6) 2017 (curettage of the site, removal of excess biomaterial contained in sinus). To date rti has received no additional information.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3002924436-2017-00013
MDR Report Key6842483
Report SourceHEALTH PROFESSIONAL
Date Received2017-09-05
Date of Report2018-03-29
Date of Event2016-07-19
Date Mfgr Received2017-08-08
Date Added to Maude2017-09-05
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationDENTIST
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMS. CHARITY EMMONS
Manufacturer Street11621 RESEARCH CIRCLE
Manufacturer CityALACHUA FL 32615
Manufacturer CountryUS
Manufacturer Postal32615
Manufacturer Phone3864188888
Manufacturer G1RTI SURGICAL
Manufacturer Street11621 RESEARCH CIRCLE
Manufacturer CityALACHUA FL 32615
Manufacturer CountryUS
Manufacturer Postal Code32615
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameCOPIOS PERICARDIUM XENOGRAFT MEMBRANES
Generic NameCOPIOS PERICARDIUM XENOGRAFT MEMBRANE
Product CodeNPL
Date Received2017-09-05
Lot NumberNZ15290088
OperatorDENTIST
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerTUTOGEN MEDICAL GMBH
Manufacturer AddressINDUSTRUESTR 6. NEUNKIRCHEN, GERMANY 91077GM GM 91077 GM


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2017-09-05

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