MAUDE Adverse Event Report: TAMBRANDS MANUFACTURING, INC TAMPAXTAMPONSPEARLPOCKETCOMPAKMIXEDUNSCNT30CT; TAMPON, MENSTRUAL, UNSCENTED - HEB

Lot Number	503924302811 20:01
Medical Device Problem Code	No Apparent Adverse Event (3189)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
Product investigation is in progress.
Event or Problem Description
String was left in the plastic tube as if it was never attached to the tampon [device physical property issue].Case narrative: consumer reported via e-mail that the tampon string was left in the tube.No injury reported.
Additional Manufacturer Narrative
No failure could be identified as a result of the investigation.
Event or Problem Description
String was left in the plastic tube as if it was never attached to the tampon [device physical property issue].Case narrative: consumer reported via e-mail that the tampon string was left in the tube.No injury reported.

• Brand Name: TAMPAXTAMPONSPEARLPOCKETCOMPAKMIXEDUNSCNT30CT
• Common Device Name: 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 Key: 22045530
• Report Number: 1219109-2025-00140
• Device Sequence Number: 18396512
• Product Code: HEB
• UDI-Device Identifier: 00073010712843
• UDI-Public: (01)00073010712843
• Combination Product (Y/N): Y
• Initial Reporter Country: US
• PMA/510(K) Number: K133244
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Consumer
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup
• Report Date (Section B): 06/23/2025

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Operator of Device: Lay User/Patient
• Device Lot Number: 503924302811 20:01
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: No
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: Not provided
• Supplement Date Received by Manufacturer: Not provided
• Initial Report FDA Received Date: 05/19/2025
• Supplement Report FDA Received Date: 06/25/2025
• Was Device Evaluated by Manufacturer? (Y/N): Device Not Returned to Manufacturer
• Is the Device Labeled for Single Use? (Y/N): No
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Initial
• Patient Sequence Number: 1
• Patient Sex: Female