PLAYTEX, GENTLE GLIDE, SUPER PLUS, SCENTED TAMPONS

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 07 report with the FDA on 2009-09-23 for PLAYTEX, GENTLE GLIDE, SUPER PLUS, SCENTED TAMPONS manufactured by Playtex Products, Inc..

Event Text Entries

[1177351] Received a report from a consumer indicating pieces of a tampon pledget separated and remained behind during removal of a tampon. Reporter advised the piece(s) expelled on their own accord within several days. No injury reported.
Patient Sequence No: 1, Text Type: D, B5


[8284365] We have requested and await consumer's return of product for eval and date code info for investigation.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number2515444-2009-00010
MDR Report Key1504923
Report Source07
Date Received2009-09-23
Date of Report2009-09-23
Date of Event2009-08-15
Date Mfgr Received2009-08-18
Date Added to Maude2010-06-24
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 FDA3
Report to FDA0
Event Location0
Manufacturer ContactJANET DEPALMA
Manufacturer Street75 COMMERCE DR
Manufacturer CityALLENDALE NJ 07401
Manufacturer CountryUS
Manufacturer Postal07401
Manufacturer Phone2017858000
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NamePLAYTEX, GENTLE GLIDE, SUPER PLUS, SCENTED TAMPONS
Generic NameTAMPON
Product CodeHIL
Date Received2009-09-23
Model NumberNA
Catalog NumberNA
Lot NumberUNK
ID NumberNA
Device AgeDA
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerPLAYTEX PRODUCTS, INC.
Manufacturer Address804 WALKER RD DOVER DE 19990 US 19990


Patients

Patient NumberTreatmentOutcomeDate
10 2009-09-23

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