ATTUNE RP PS ARTIC SURF SZ8 254500548

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2019-05-16 for ATTUNE RP PS ARTIC SURF SZ8 254500548 manufactured by Depuy Ireland 9616671.

Event Text Entries

[145295220] (b)(4). If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.
Patient Sequence No: 1, Text Type: N, H10


[145295221] It was reported that during trialing, the physician`s assistant accidentally put a little too much pressure on one of the posts with the retention spring and it broke off. Both pieces were recovered and did not delay the case.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1818910-2019-93746
MDR Report Key8617419
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2019-05-16
Date of Report2019-04-25
Date of Event2019-04-25
Date Mfgr Received2019-06-06
Device Manufacturer Date2014-03-14
Date Added to Maude2019-05-16
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional0
Initial Report to FDA0
Report to FDA3
Event Location3
Manufacturer ContactMS. KARA DITTY-BOVARD
Manufacturer Street1210 WARD AVENUE
Manufacturer CityWEST CHESTER PA 193800988
Manufacturer CountryUS
Manufacturer Postal193800988
Manufacturer Phone6103142063
Manufacturer G1DEPUY ORTHOPAEDICS, INC. 1818910
Manufacturer Street700 ORTHOPAEDIC DRIVE
Manufacturer CityWARSAW IN 465820988
Manufacturer CountryUS
Manufacturer Postal Code465820988
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameATTUNE RP PS ARTIC SURF SZ8
Generic NameATTUNE INSTRUMENTS : TIBIAL TRIALS
Product CodeKWH
Date Received2019-05-16
Returned To Mfg2019-05-15
Catalog Number254500548
Lot NumberMVMBSV750
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerDEPUY IRELAND 9616671
Manufacturer AddressLOUGHBEG, RINGASKIDDY CO. CORK EI


Patients

Patient NumberTreatmentOutcomeDate
10 2019-05-16

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