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Tampax Tampax Pearl (UDI 00073010479050)Recalls & reported problems

Procter & Gamble Manufacturing Company, The · TAMPAX PEARL SUPER PLUS 18CT · Class 2

All models of Tampax (40)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
4
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00073010479050), received between Jan 9, 2025 and Feb 14, 2026 — classified as 4 malfunctions.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (2 reports).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Reports received per month

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 1 reportsFeb 2025: 1 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 1 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 1 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520261
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Insufficient Device Problem Information2
  • No Apparent Adverse Event2
  • Adverse Event Without Identified Device or Use Problem1

Patient problems

  • Foreign Body In Patient2
  • No Clinical Signs, Symptoms or Conditions2
  • Unspecified Infection1

Recent adverse event reports

The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

  • MalfunctionFeb 14, 2026Insufficient Device Problem Information

    INFECTION - VAGINAL [VAGINAL INFECTION]. LEFT PIECES OF THE COTTON AND STRING INSIDE ME; EMERGENCY ROOM FOUND 2 MORE LONG PIECES WAY UP INSIDE VAGINA [FOREIGN BODY IN REPRODUCTIVE TRACT]. FALLEN APART - TAMPAX [DEVICE BREAKAGE]. I'M REMOVING THE TAMPON. IT HAD FALLEN APART INSIDE MY VAGINA AND LEFT PIECES OF COTTON AND STRING INSIDE [COMPLICATION OF DEVICE REMOVAL]. CASE NARRATIVE: CONSUMER REPORTED VIA E-MAIL THAT THE TAMPON HAS FALLEN APART INSIDE HER. NO SERIOUS INJURY REPORTED.

    Patient problems: Foreign Body In Patient; Unspecified Infection

    MAUDE report 24340378 ↗
  • MalfunctionJun 20, 2025No Apparent Adverse Event; No Apparent Adverse Event

    SEVERAL LITTLE PIECES BROKE OFF THE SIDE- TAMPAX TAMPON [DEVICE BREAKAGE] CASE NARRATIVE: RELATIVE REPORTED VIA SOCIAL MEDIA THAT SEVERAL PIECES BROKE OFF THE TAMPON WHILE CONSUMER WAS REMOVING IT. NO INJURY WAS REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 22298417 ↗
  • MalfunctionFeb 25, 2025No Apparent Adverse Event; No Apparent Adverse Event

    STRINGS WERE ALREADY DETACHED OR JUST HANGING ON BY A THREAD- TAMPON [DEVICE PHYSICAL PROPERTY ISSUE]. PROBABLE MANUFACTURING CAUSE [MANUFACTURING ISSUE]. CASE NARRATIVE: CONSUMER REPORTED VIA E-MAIL THAT THE TAMPON STRINGS WERE ALREADY DETACHED OR HANGING ON BY A THREAD. NO INJURY REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 21459816 ↗
  • MalfunctionJan 9, 2025Adverse Event Without Identified Device or Use Problem; Insufficient Device Problem Information; Adverse Event Without Identified Device or Use Problem; Insufficient Device Problem Information

    COTTON IS COMING APART INSIDE OF ME- VAGINA [FOREIGN BODY IN REPRODUCTIVE TRACT], COTTON IS COMING APART [DEVICE BREAKAGE] , WHEN I GO TO CHANGE MY TAMPON, THE COTTON IS COMING APART INSIDE OF ME [COMPLICATION OF DEVICE REMOVAL] . CASE NARRATIVE: CONSUMER REPORTED VIA E-MAIL THAT THE COTTON IS COMING APART INSIDE. NO SERIOUS INJURY REPORTED.

    Patient problems: Foreign Body In Patient

    MAUDE report 21111499 ↗

Other TAMPON, MENSTRUAL, UNSCENTED devices

All TAMPON, MENSTRUAL, UNSCENTED devices →

Sources and updates

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