ATTUNE MEDIAL ANAT PAT 32MM 151810032

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 2019-11-06 for ATTUNE MEDIAL ANAT PAT 32MM 151810032 manufactured by Depuy Ireland - 9616671.

Event Text Entries

[167349182] (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


[167349183] It was reported that patient had a quad tendon repair 2 years post joint replacement. Surgical site became infected and spread to total joint requiring extraction and implantation of antibiotic spacer. Doi: (b)(6) 2017; dor: (b)(6) 2019; right knee.
Patient Sequence No: 1, Text Type: D, B5


[185847632] Product complaint # (b)(4). Investigation summary ==> the device associated with this report was not received for examination. Depuy synthes considers the investigation closed at this time. Should additional information be received, the information will be reviewed and the investigation may be re-opened as necessary. 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


MAUDE Entry Details

Report Number1818910-2019-114470
MDR Report Key9285138
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2019-11-06
Date of Report2019-10-11
Date of Event2019-10-11
Date Mfgr Received2019-10-11
Device Manufacturer Date2017-03-13
Date Added to Maude2019-11-06
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactKARA DITTY-BOVARD
Manufacturer Street700 ORTHOPAEDIC DR.
Manufacturer CityWARSAW IN 465810988
Manufacturer CountryUS
Manufacturer Postal465810988
Manufacturer Phone6107428552
Manufacturer G1DEPUY IRELAND - 9616671
Manufacturer StreetLOUGHBEG RINGASKIDDY CO.
Manufacturer CityCORK
Manufacturer CountryEI
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameATTUNE MEDIAL ANAT PAT 32MM
Generic NameATTUNE IMPLANT : KNEE PATELLA
Product CodeKWH
Date Received2019-11-06
Catalog Number151810032
Lot Number8490601
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerDEPUY IRELAND - 9616671
Manufacturer AddressLOUGHBEG RINGASKIDDY CO. CORK EI


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2019-11-06

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