ALWAYS INFINITY PAD

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2015-03-12 for ALWAYS INFINITY PAD manufactured by Procter And Gamble.

Event Text Entries

[21540174] Rash/itchiness, severe irritation to area in contact with edges of feminine pad (question reaction to adhesive used in product).
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report NumberMW5041503
MDR Report Key4614033
Date Received2015-03-12
Date of Report2015-03-12
Date of Event2015-02-19
Date Added to Maude2015-03-19
Event Key0
Report Source CodeVoluntary report
Manufacturer LinkN
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag0
Reporter OccupationPATIENT
Health Professional0
Initial Report to FDA3
Report to FDA0
Event Location0
Single Use0
Previous Use Code0
Event Type3
Type of Report3

Device Sequence Number: 1

Brand NameALWAYS INFINITY PAD
Generic NameALWAYS INFINITY PAD
Product CodeHHD
Date Received2015-03-12
Device AvailabilityY
Device Sequence No1
Device Event Key0
ManufacturerPROCTER AND GAMBLE

Device Sequence Number: 2

Brand NameALWAYS ALL DAY PANTY LINER
Generic NamePANTY LINER
Product CodeHHD
Date Received2015-03-12
OperatorHEALTH PROFESSIONAL
Device Sequence No2
Device Event Key0
ManufacturerPROCTER AND GAMBLE


Patients

Patient NumberTreatmentOutcomeDate
10 2015-03-12

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