MEPILEX BORDER POST-OP AG 498600

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2020-01-15 for MEPILEX BORDER POST-OP AG 498600 manufactured by Molnlycke Healthcare.

Event Text Entries

[175666594] Mepilex border post-op ag dressing opened onto surgical field where it was noted to be discolored exchanged for a different "like" dressing. Fda safety report id# (b)(4).
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report NumberMW5092284
MDR Report Key9596114
Date Received2020-01-15
Date of Report2020-01-13
Date of Event2020-01-13
Date Added to Maude2020-01-16
Event Key0
Report Source CodeVoluntary report
Manufacturer LinkN
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
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameMEPILEX BORDER POST-OP AG
Generic NameDRESSING, WOUND, DRUG
Product CodeFRO
Date Received2020-01-15
Model Number498600
Catalog Number498600
Lot Number19187779
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by MfgrI
Device Sequence No1
Device Event Key0
ManufacturerMOLNLYCKE HEALTHCARE
Manufacturer AddressNORCROSS GA 30092 US 30092


Patients

Patient NumberTreatmentOutcomeDate
10 2020-01-15

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