EXCEED ABT E1 N/FLNG CUP 32X50 N/A EP-113250

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,other report with the FDA on 2019-03-14 for EXCEED ABT E1 N/FLNG CUP 32X50 N/A EP-113250 manufactured by Biomet Uk Ltd..

Event Text Entries

[138762494] (b)(4). Concomitant medical products: 32mm diameter -3. 5mm neck length, catalog #: 00-8018-32-01, lot #: 63562615. Report source, foreign - event occurred in the (b)(6). Reported event was unable to be confirmed due to limited information received from the customer. Device history record (dhr) was reviewed and no discrepancies were found. Root cause was unable to be determined as the necessary information to adequately investigate the reported event was not provided. If any further information is found which would change or alter any conclusions or information, a supplemental will be filed accordingly. Zimmer biomet will continue to monitor for trends.
Patient Sequence No: 1, Text Type: N, H10


[138762495] Hip revision due to dislocation and subluxation.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3002806535-2019-00276
MDR Report Key8419834
Report SourceFOREIGN,OTHER
Date Received2019-03-14
Date of Report2019-03-14
Date of Event2018-05-23
Date Mfgr Received2019-02-14
Device Manufacturer Date2017-05-30
Date Added to Maude2019-03-14
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 NameEXCEED ABT E1 N/FLNG CUP 32X50
Generic NameHIP PROSTHESIS
Product CodeJDD
Date Received2019-03-14
Model NumberN/A
Catalog NumberEP-113250
Lot Number6053907
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerBIOMET UK LTD.
Manufacturer AddressWATERTON INDUSTRIAL ESTATES BRIDGEND CF313XA UK CF31 3XA


Patients

Patient NumberTreatmentOutcomeDate
101. Hospitalization; 2. Required No Informationntervention 2019-03-14

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