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Tampax Tampax Pearl (UDI 00073010711358)Recalls & reported problems

Procter & Gamble Manufacturing Company, The · TAMPAX PEARL REGULAR 50CT · Class 2

All models of Tampax (40)

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

Adverse event reports
7
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 00073010711358), received between May 28, 2024 and Apr 16, 2026 — classified as 1 injury, 6 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: 1 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: 0 reportsMar 2025: 0 reportsApr 2025: 1 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 1 reportsNov 2025: 1 reportsDec 2025: 0 reportsJan 2026: 1 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 1 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 Information3
  • No Apparent Adverse Event3
  • Product Quality Problem2
  • Adverse Event Without Identified Device or Use Problem1
  • Patient-Device Incompatibility1

Patient problems

  • No Clinical Signs, Symptoms or Conditions3
  • Foreign Body In Patient2
  • Anxiety1
  • Burning Sensation1
  • Discomfort1
  • Fever1
  • Hypersensitivity/Allergic reaction1
  • Itching Sensation1

Recent adverse event reports

The 7 most recent of 7 reports, in the reporter's own words as published by the FDA.

  • MalfunctionApr 16, 2026No Apparent Adverse Event

    THE STRING BREAKS- TAMPON [DEVICE BREAKAGE]. PROBABLE MANUFACTURING CAUSE [MANUFACTURING ISSUE]. CASE NARRATIVE: CONSUMER REPORTED VIA E-MAIL THAT THE TAMPON STRING BREAKS. NO INJURY REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 24896805 ↗
  • MalfunctionJan 21, 2026No Apparent Adverse Event

    BROKEN STRINGS - TAMPON [DEVICE BREAKAGE]. CASE NARRATIVE: CONSUMER REPORTED VIA EMAIL THAT THE TAMPON STRINGS WERE BROKEN. NO INJURY REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 24134980 ↗
  • MalfunctionNov 5, 2025Product Quality Problem; Insufficient Device Problem Information; Product Quality Problem; Insufficient Device Problem Information

    THE TAMPON IS STILL IN MY BODY, VAGINA [FOREIGN BODY IN REPRODUCTIVE TRACT]. STRINGS BROKEN OFF OR FRAYED [DEVICE BREAKAGE]. PROBABLE MANUFACTURING CAUSE [MANUFACTURING ISSUE]. CASE NARRATIVE: CONSUMER REPORTED VIA E-MAIL THAT THE TAMPON STRINGS ARE BROKEN OFF AND FRAYED. NO SERIOUS INJURY REPORTED.

    Patient problems: Foreign Body In Patient

    MAUDE report 23474596 ↗
  • MalfunctionOct 15, 2025Product Quality Problem; Insufficient Device Problem Information; Product Quality Problem; Insufficient Device Problem Information

    ANXIETY MIND [ANXIETY]. DISCOMFORT VAGINA [VULVOVAGINAL DISCOMFORT] . ENTIRE BOX, FAULTY STRINGS ARE HALF CUT [DEVICE PHYSICAL PROPERTY ISSUE] . STRINGS SNAP RIGHT OFF- TAMPON [DEVICE BREAKAGE] . PROBABLE MANUFACTURING CAUSE [MANUFACTURING ISSUE] . CASE NARRATIVE: CONSUMER REPORTED VIA E-MAIL THAT THE STRINGS ARE HALF CUT AND SNAP OFF. NO SERIOUS INJURY REPORTED.

    Patient problems: Anxiety; Discomfort

    MAUDE report 23303906 ↗
  • InjuryApr 10, 2025Patient-Device Incompatibility

    UPON USING REGULAR TAMPAX PEARL DEVELOPED SKIN AND VAGINAL IRRITATION, ITCHING, AND BURNING. INITIAL OCCURRENCE IN MARCH SELF-DIAGNOSED AS YEAST INFECTION DAY TWO OF PERIOD AND TREATED WITH OVER COUNTER MEDICINE & CREAM, QUIT USING PRODUCT. OVER COUNTER CREAM EASED PAIN BUT DID NOT CLEAR SYMPTOMS IN DESIGNATED TIME. SECOND OCCURRENCE WITH SAME ONSET OF SYMPTOMS AND TIMING SOUGHT MEDICAL CARE. YEAST INFECTION, UTI, AND BACTERIAL VAGINOSIS ALL RULED OUT VIA LAB TESTS. DIAGNOSED AS PROBABLE ALLERGIC REACTION TO TAMPONS USED.

    Patient problems: Burning Sensation; Hypersensitivity/Allergic reaction; Itching Sensation

    MAUDE report 21814992 ↗
  • MalfunctionJan 30, 2025Adverse Event Without Identified Device or Use Problem; Insufficient Device Problem Information; Adverse Event Without Identified Device or Use Problem; Insufficient Device Problem Information

    HAD TO GO TO URGENT CARE TO HAVE THE TAMPON FISHED OUT OF ME- VAGINA [FOREIGN BODY IN REPRODUCTIVE TRACT] . I THINK I HAVE A FEVER [PYREXIA] . I HAD A TAMPON THAT I WAS TRYING TO TAKE OUT WHEN THE STRING RIPPED OFF...HAVING TO GO TO URGENT CARE TO HAVE THE TAMPON FISHED OUT [COMPLICATION OF DEVICE REMOVAL] . STRING RIPPED COMPLETELY OFF- TAMPON [DEVICE BREAKAGE] . CASE NARRATIVE: CONSUMER REPORTED VIA E-MAIL THAT THE TAMPON STRING RIPPED OFF DURING REMOVAL. NO SERIOUS INJURY REPORTED.

    Patient problems: Fever; Foreign Body In Patient

    MAUDE report 21276189 ↗
  • MalfunctionMay 28, 2024No Apparent Adverse Event; No Apparent Adverse Event

    THE STRINGS FALLS OFF [DEVICE BREAKAGE]. CASE NARRATIVE: CONSUMER REPORTED VIA PHONE THAT THE TAMPON STRINGS FALL OFF. NO INJURY WAS REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 19404998 ↗

Other TAMPON, MENSTRUAL, UNSCENTED devices

All TAMPON, MENSTRUAL, UNSCENTED devices →

Sources and updates

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