EPICEL (CULTURED EPIDERMAL AUTOGRAFTS) GRAFT UNK

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,07 report with the FDA on 2012-04-23 for EPICEL (CULTURED EPIDERMAL AUTOGRAFTS) GRAFT UNK manufactured by Genzyme Biosurgery (cambridge).

Event Text Entries

[2688959] Death [death]. Case description. Spontaneous report was received on (b)(6) 2012, from a physician (via a company representative) regarding a pt, initials (b)(6). The pt's medical history was not provided. On (b)(6) 2012, the pt was grafted with 48 epicel grafts. On (b)(6) 2012, the pt expired. The action taken with epicel treatment was not provided. Concomitant medications were not provided. The relationship between epicel and the event of death was not provided by the reporting physician.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1226230-2012-00001
MDR Report Key2556443
Report Source05,07
Date Received2012-04-23
Date of Report2012-04-13
Date Mfgr Received2012-04-13
Date Added to Maude2012-05-03
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 FDA3
Event Location0
Manufacturer ContactJILL ROBINSON, R. PH, MBA
Manufacturer Street675 WEST KENDALL STREET
Manufacturer CityCAMBRIDGE MA 02142
Manufacturer CountryUS
Manufacturer Postal02142
Manufacturer Phone6177689000
Manufacturer G1GENZYME BIOSURGERY (CAMBRIDGE)
Manufacturer Street64 SIDNEY ST.
Manufacturer CityCAMBRIDGE MA 02139
Manufacturer CountryUS
Manufacturer Postal Code02139
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameEPICEL (CULTURED EPIDERMAL AUTOGRAFTS) GRAFT
Generic NameCULTURED EPIDERMAL AUTOGRAFTS
Product CodeOCE
Date Received2012-04-23
Model NumberUNK
Catalog NumberUNK
Lot NumberEE01597
ID NumberUNK
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerGENZYME BIOSURGERY (CAMBRIDGE)
Manufacturer AddressCAMBRIDGE MA US


Patients

Patient NumberTreatmentOutcomeDate
101. Death 2012-04-23

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