EUFLEXXA 6301182010

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 2020-03-16 for EUFLEXXA 6301182010 manufactured by Bio-technology General (israel) Ltd..

Event Text Entries

[183653128] Lost balance [balance disorder]. Had fallen and broken her arm [fall]. Had fallen and broken her arm [upper limb fracture] case (b)(4) is a serious spontaneous case received from a non-health professional via regulatory authority in united states. This report concerns a female of an unknown age who had lost balance, had fallen and broken her arm during treatment with intra-articular euflexxa (sodium hyaluronate) solution for injection 10 mg, unknown dose, route and frequency, for an unknown indication from an unknown start date to an unknown stop date. The patient had lost balance, had fallen and broken her arm. The patient was hospitalized on an unknown date due to lost balance, had fallen and broken her arm. Action taken with euflexxa was unknown. At the time of this report, the outcome of lost balance, had fallen and broken her arm was unknown no concomitant medication was reported. All events in the case were reported as serious. At the time of reporting the case outcome was unknown. Ferring's sender comment: association of euflexxa to lost balance, fall, and broken her arm events are considered unrelated due to lack of biological plausibility. Overall listedness (core label) is unlisted. Reporter causality: related company causality: not related other case numbers: internal # - others = mw5092963 this ae occurred in the us and concerns the medical device euflexxa. Please report to your local health authority if required by local law. This ae is not reportable in eu because it did not occur in a eu + efta country and did not result in a corrective action by the manufacturer no corrective action was done by the manufacturer or requested by regulators.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3000164186-2020-00006
MDR Report Key9836776
Report SourceHEALTH PROFESSIONAL
Date Received2020-03-16
Date of Report2020-03-16
Date of Event2019-12-20
Date Mfgr Received2020-03-03
Date Added to Maude2020-03-16
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer Street100 INTERPACE PARKWAY
Manufacturer CityPARSIPPANY, NJ
Manufacturer CountryUS
Manufacturer Phone3044828
Manufacturer G1BIO-TECHNOLOGY GENERAL (ISRAEL) LTD.
Manufacturer StreetBE'ER TUVIA INDUSTRIAL ZONE POB 571
Manufacturer CityKIRYAT MALACHI, 83104
Manufacturer CountryIS
Manufacturer Postal Code83104
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameEUFLEXXA
Generic Name1% SODIUM HYALURONATE
Product CodeMOZ
Date Received2020-03-16
Catalog Number6301182010
Lot NumberL14134A
Device AvailabilityN
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerBIO-TECHNOLOGY GENERAL (ISRAEL) LTD.
Manufacturer AddressBE'ER TUVIA INDUSTRIAL ZONE POB 571 KIRYAT MALACHI, 83104 IS 83104


Patients

Patient NumberTreatmentOutcomeDate
101. Hospitalization 2020-03-16

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