ALWAYS PAD, VERSION/ABSORBENCY/SCENT UNKNOWN (NOT APPLICABLE) PAD 1 APPLIC

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 04 report with the FDA on 2012-11-21 for ALWAYS PAD, VERSION/ABSORBENCY/SCENT UNKNOWN (NOT APPLICABLE) PAD 1 APPLIC manufactured by Procter & Gamble, Inc..

Event Text Entries

[3041947] Event verbatim [preferred term] (related symptoms if any separated by commas): rash from pad [rash]. Case description: a consumer reported that her daughter, age unspecified, used always pad, version/absorbency/scent unknown and reported that her daughter developed a rash that became so bad she was admitted to the hospital for approximately 1 week and treated with an unspecified cream. The case outcome was improved. No further information was provided.
Patient Sequence No: 1, Text Type: D, B5


[10341372] Lot number was provided by the reporter but product was not available for return therefore batch retain investigation requested and results pending.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number8022168-2012-00001
MDR Report Key2848251
Report Source04
Date Received2012-11-21
Date of Report2012-10-25
Date Mfgr Received2012-10-25
Date Added to Maude2012-11-29
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag0
Health Professional0
Initial Report to FDA0
Report to FDA3
Event Location0
Manufacturer ContactMGR.
Manufacturer Street6110 CENTER HILL AVE. WINTON HILL BUSINESS CTR.
Manufacturer CityCINCINNATI OH 45224
Manufacturer CountryUS
Manufacturer Postal45224
Manufacturer G1PROCTER & GAMBLE, INC.
Manufacturer Street355 UNIVERSITY AVE.
Manufacturer CityBELLEVILLE, ONTARIO K8N5E9
Manufacturer CountryCA
Manufacturer Postal CodeK8N5E9
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameALWAYS PAD, VERSION/ABSORBENCY/SCENT UNKNOWN (NOT APPLICABLE) PAD 1 APPLIC
Generic NameNONE
Product CodeHHD
Date Received2012-11-21
OperatorLAY USER/PATIENT
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerPROCTER & GAMBLE, INC.
Manufacturer AddressBELLEVILLE, ONTARIO CA


Patients

Patient NumberTreatmentOutcomeDate
101. Hospitalization; 2. Other 2012-11-21

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