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Tampax Tampax Pearl (UDI 00073010004559)Recalls & reported problems

Procter & Gamble Manufacturing Company, The · TAMPAX PEARL REGULAR 36CT · 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 00073010004559), received between Feb 10, 2026 and Sep 29, 2026 — classified as 4 malfunctions.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (3 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: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 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: 2 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 1 reportsOct 2026: 0 reports2024202520262
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Insufficient Device Problem Information3
  • No Apparent Adverse Event1
  • Product Quality Problem1

Patient problems

  • Foreign Body In Patient3
  • Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available2
  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

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

  • MalfunctionSep 29, 2026No Apparent Adverse Event

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50928808 ↗
  • MalfunctionMay 21, 2026Insufficient Device Problem Information

    [TAMPON] LEAVING A LARGE AMOUNT OF THE FIBERS INSIDE OF ME - VAGINA [FOREIGN BODY IN REPRODUCTIVE TRACT] PAIN VAGINA [VULVOVAGINAL PAIN]. VAGINAL DRYNESS [VULVOVAGINAL DRYNESS]. REMOVING [TAMPON]... LEAVING A LARGE AMOUNT OF THE FIBERS INSIDE OF ME [COMPLICATION OF DEVICE REMOVAL]. TORE - TAMPON [DEVICE BREAKAGE]. CASE NARRATIVE: CONSUMER REPORTED VIA E-MAIL THAT TAMPON TORE DURING REMOVAL. NO SERIOUS INJURY WAS REPORTED.

    Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available; Foreign Body In Patient

    MAUDE report 25239334 ↗
  • MalfunctionMay 4, 2026Insufficient Device Problem Information

    COTTON ON THE INSIDE TORE, LEAVING PIECES BEHIND - TAMPON [FOREIGN BODY IN REPRODUCTIVE TRACT]. COTTON ON THE INSIDE TORE AND SHREDDED AS I PULLED IT OUT, LEAVING PIECES BEHIND - TAMPON [COMPLICATION OF DEVICE REMOVAL]. COTTON ON THE INSIDE TORE AND SHREDDED - TAMPON [DEVICE BREAKAGE]. CASE NARRATIVE: CONSUMER REPORTED VIA PHONE THAT THE TAMPON TORE AND SHREDDED DURING REMOVAL. NO SERIOUS INJURY WAS REPORTED.

    Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available; Foreign Body In Patient

    MAUDE report 25064808 ↗
  • MalfunctionFeb 10, 2026Product Quality Problem; Insufficient Device Problem Information

    STRING BROKE OFF SO I HAD TO DIG TO GET IT OUT- VAGINA [FOREIGN BODY IN REPRODUCTIVE TRACT] STRING BROKE OFF- TAMPON [DEVICE BREAKAGE] . PROBABLE MANUFACTURING CAUSE [MANUFACTURING ISSUE] . CASE NARRATIVE: CONSUMER REPORTED VIA E-MAIL THAT THE STRING BROKE OFF. NO SERIOUS INJURY REPORTED.

    Patient problems: Foreign Body In Patient

    MAUDE report 24304707 ↗

Other TAMPON, MENSTRUAL, UNSCENTED devices

All TAMPON, MENSTRUAL, UNSCENTED devices →

Sources and updates

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