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..
[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
Report Number | 2515444-2009-00010 |
MDR Report Key | 1504923 |
Report Source | 07 |
Date Received | 2009-09-23 |
Date of Report | 2009-09-23 |
Date of Event | 2009-08-15 |
Date Mfgr Received | 2009-08-18 |
Date Added to Maude | 2010-06-24 |
Event Key | 0 |
Report Source Code | Manufacturer report |
Manufacturer Link | Y |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 0 |
Health Professional | 0 |
Initial Report to FDA | 3 |
Report to FDA | 0 |
Event Location | 0 |
Manufacturer Contact | JANET DEPALMA |
Manufacturer Street | 75 COMMERCE DR |
Manufacturer City | ALLENDALE NJ 07401 |
Manufacturer Country | US |
Manufacturer Postal | 07401 |
Manufacturer Phone | 2017858000 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | PLAYTEX, GENTLE GLIDE, SUPER PLUS, SCENTED TAMPONS |
Generic Name | TAMPON |
Product Code | HIL |
Date Received | 2009-09-23 |
Model Number | NA |
Catalog Number | NA |
Lot Number | UNK |
ID Number | NA |
Device Age | DA |
Device Eval'ed by Mfgr | * |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | PLAYTEX PRODUCTS, INC. |
Manufacturer Address | 804 WALKER RD DOVER DE 19990 US 19990 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2009-09-23 |