LIQUIBAND EXCEED

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor report with the FDA on 2020-02-27 for LIQUIBAND EXCEED manufactured by Advanced Medical Solutions Limited.

Event Text Entries

[181479723] "insufficient information provided and at this time we are unable to confirm if the device caused or contributed to a serious injury. If further information becomes available a follow-up report will be submitted. "
Patient Sequence No: 1, Text Type: N, H10


[181479724] Skin reaction.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9617175-2020-00015
MDR Report Key9763393
Report SourceDISTRIBUTOR
Date Received2020-02-27
Date of Report2020-02-27
Date Mfgr Received2020-02-07
Date Added to Maude2020-02-27
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 StreetWESTERN WOOD WAY LANGAGE SCIENCE PARK
Manufacturer CityPLYMPTON, PL75BG
Manufacturer CountryUK
Manufacturer PostalPL75BG
Manufacturer G1ADVANCED MEDICAL SOLUTIONS LIMITED
Manufacturer StreetWESTERN WOOD WAY LANGAGE SCIENCE PARK
Manufacturer CityPLYMPTON, PL75BG
Manufacturer CountryUK
Manufacturer Postal CodePL75BG
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameLIQUIBAND EXCEED
Generic NameTOPICAL SKIN ADHESIVE
Product CodeMPN
Date Received2020-02-27
Device Availability*
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerADVANCED MEDICAL SOLUTIONS LIMITED
Manufacturer AddressWESTERN WOOD WAY LANGAGE SCIENCE PARK PLYMPTON, PL75BG UK PL75BG


Patients

Patient NumberTreatmentOutcomeDate
10 2020-02-27

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