FLEXHD, 16CM X 20CM/MTF - HUMAN ALLOGRAFT 471620

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,06 report with the FDA on 2011-07-22 for FLEXHD, 16CM X 20CM/MTF - HUMAN ALLOGRAFT 471620 manufactured by .

Event Text Entries

[2140203] On (b)(6) 2011, the pt underwent breast implant and fat grafting surgery, was implanted with the allograft, and discharged the same day. It was reported that following surgery (date unk), she developed inflammation. The wound was opened, cultured, and packed. The cultures were negative for growth. The pt was prescribed antibiotics and is recovering. Note: third adverse event referenced in a single report received from this facility. Allograft serial number and incident details were not provided until (b)(6) 2011.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3001236616-2011-00020
MDR Report Key2177017
Report Source05,06
Date Received2011-07-22
Date of Report2011-07-11
Date of Event2011-03-01
Date Mfgr Received2011-06-15
Date Added to Maude2011-07-26
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag0
Health Professional3
Initial Report to FDA3
Report to FDA0
Event Location0
Manufacturer ContactNINA ONYSZCZUK
Manufacturer Street125 MAY STREET, STE 300
Manufacturer CityEDISON NJ 08837
Manufacturer CountryUS
Manufacturer Postal08837
Manufacturer Phone7326614064
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameFLEXHD, 16CM X 20CM/MTF - HUMAN ALLOGRAFT
Generic NameNONE
Product CodeLMO
Date Received2011-07-22
Catalog Number471620
Lot Number0850910432
ID Number1004A
Device Expiration Date2013-05-27
Device AgeDA
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2011-07-22

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