NUT

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 01,07 report with the FDA on 2012-10-24 for NUT manufactured by Synthes Usa.

Event Text Entries

[3016755] Device report from (b)(4) reports an event in (b)(6) as follows: patient underwent removal of rods and screws - t12-s1. Revision fusion, repair pseudoarthrosis l3-l4. Re-instrumentation t12-pelvis on (b)(6) 2010. This is #31 of 44 reports for the same event.
Patient Sequence No: 1, Text Type: D, B5


[10382080] Additional narrative: device was used for treatment. Report originally received (b)(4) 2012; further evaluation revealed 43 additional devices within the reported event which were identified on (b)(4) 2012. Investigation could not be completed, no conclusion could be drawn as device was not returned and lot number was not provided.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number2520274-2012-02554
MDR Report Key2802877
Report Source01,07
Date Received2012-10-24
Date of Report2012-08-29
Date Mfgr Received2012-08-29
Date Added to Maude2012-10-24
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 FDA0
Event Location0
Manufacturer ContactSARMA PIN
Manufacturer Street1302 WRIGHTS LANE EAST
Manufacturer CityWEST CHESTER PA 19380
Manufacturer CountryUS
Manufacturer Postal19380
Manufacturer Phone8006207025
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Generic NameNUT
Product CodeLYT
Date Received2012-10-24
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerSYNTHES USA
Manufacturer Address1302 WRIGHTS LANE EAST WEST CHESTER PA 19380 19380


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2012-10-24

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