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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: TAMBRANDS MANUFACTURING, INC TAMPAX TAMPON, VERSION/ABSORBENCY/SCENT UNKNOWN; TAMPON, MENSTRUAL, UNSCENTED - HEB

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TAMBRANDS MANUFACTURING, INC TAMPAX TAMPON, VERSION/ABSORBENCY/SCENT UNKNOWN; TAMPON, MENSTRUAL, UNSCENTED - HEB Back to Search Results
Device Problem No Apparent Adverse Event (3189)
Patient Problem No Clinical Signs, Symptoms or Conditions (4582)
Event Type  malfunction  
Event Description
Tampon leaving chunks behind, falling apart [device breakage].Case narrative: consumer reported via e-mail that the tampon is leaving chunks behind and falling apart during use.No injury reported.
 
Manufacturer Narrative
There is insufficient information to perform an investigation.
 
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Brand Name
TAMPAX TAMPON, VERSION/ABSORBENCY/SCENT UNKNOWN
Type of Device
TAMPON, MENSTRUAL, UNSCENTED - HEB
Manufacturer (Section D)
TAMBRANDS MANUFACTURING, INC
2879 hotel rd
auburn 04210
Manufacturer (Section G)
TAMBRANDS MANUFACTURING, INC
2879 hotel rd
auburn 04210
Manufacturer Contact
manager affairs,feminine care
winton hill business center b
6280 center hill avenue
cincinnati 45224
MDR Report Key18923706
MDR Text Key337899580
Report Number1219109-2024-00074
Device Sequence Number1
Product Code HEB
Combination Product (y/n)Y
Reporter Country CodeUS
PMA/PMN Number
K081555
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type Consumer
Reporter Occupation Other
Type of Report Initial
Report Date 02/28/2024
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received03/18/2024
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator Lay User/Patient
Was Device Available for Evaluation? No
Was Device Evaluated by Manufacturer? Device Not Returned to Manufacturer
Is the Device Single Use? Yes
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Initial
Patient Sequence Number1
Patient SexFemale
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