OXF ANAT BRG LT MD SIZE 4 PMA N/A 159548

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2020-01-09 for OXF ANAT BRG LT MD SIZE 4 PMA N/A 159548 manufactured by ..

Event Text Entries

[174272859] (b)(4). Concomitant medical products: medical product: oxf uni tib tray sz c lm pma catalog #: 154722, lot #: 971290, medical product: oxf twin-peg cmntd fem md pma, catalog #: 161469, lot #: 387840. Multiple mdr reports were filed for this event, please see associated reports: 3002806535-2020-0009, 3002806535-2020- 00011. The investigation is in process. Once the investigation has been completed, a follow-up mdr will be submitted. Product not returned.
Patient Sequence No: 1, Text Type: N, H10


[174272860] It was reported that a patient underwent an initial left knee arthroplasty. Subsequently, a revision procedure due to pain was performed.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3002806535-2020-00011
MDR Report Key9568025
Report SourceHEALTH PROFESSIONAL
Date Received2020-01-09
Date of Report2020-02-06
Date of Event2019-12-11
Date Mfgr Received2020-01-28
Device Manufacturer Date2018-03-25
Date Added to Maude2020-01-09
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 FDA3
Event Location3
Manufacturer ContactMS. CHRISTINA ARNT
Manufacturer Street56 E. BELL DR.
Manufacturer CityWARSAW IN 46582
Manufacturer CountryUS
Manufacturer Postal46582
Manufacturer Phone5745273773
Manufacturer G1BIOMET UK LTD.
Manufacturer StreetWATERTON INDUSTRIAL ESTATES
Manufacturer CityBRIDGEND CF313XA
Manufacturer CountryUK
Manufacturer Postal CodeCF31 3XA
Single Use3
Previous Use Code3
Removal Correction NumberN/A
Event Type3
Type of Report3

Device Details

Brand NameOXF ANAT BRG LT MD SIZE 4 PMA
Generic NameKNEE PROTHESIS
Product CodeNRA
Date Received2020-01-09
Model NumberN/A
Catalog Number159548
Lot Number276170
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
Manufacturer.
Manufacturer AddressWATERTON INDUSTRIAL ESTATES BRIDGEND CF313XA UK CF31 3XA


Patients

Patient NumberTreatmentOutcomeDate
101. Hospitalization; 2. Required No Informationntervention 2020-01-09

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