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Tampax Tampax Pearl (UDI 00073010719972)Recalls & reported problems

Procter & Gamble Manufacturing Company, The · Tampax Pearl Regular, Super · Class 2

All models of Tampax (40)

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

Adverse event reports
2
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00073010719972), received between Jun 16, 2025 and Mar 12, 2026 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (1 report).

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: 1 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 1 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

  • Adverse Event Without Identified Device or Use Problem2
  • Insufficient Device Problem Information1

Patient problems

  • Foreign Body In Patient2
  • Discomfort1
  • Pain1

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • MalfunctionMar 12, 2026Adverse Event Without Identified Device or Use Problem; Insufficient Device Problem Information

    THERE WERE ACTUALLY FIBERS LEFT - VAGINA [FOREIGN BODY IN REPRODUCTIVE TRACT]. THERE WERE ACTUALLY FIBERS LEFT FROM ME PULLING IT OUT - TAMPON [COMPLICATION OF DEVICE REMOVAL]. ALMOST FALLING APART. THERE WERE ACTUALLY FIBERS LEFT - TAMPON [DEVICE BREAKAGE]. CASE NARRATIVE: CONSUMER REPORTED VIA E-MAIL THAT THE TAMPON WAS ALMOST FALLING APART, AND THERE WERE FIBERS LEFT FROM HER PULLING IT OUT. NO SERIOUS INJURY REPORTED.

    Patient problems: Foreign Body In Patient

    MAUDE report 24581799 ↗
  • MalfunctionJun 16, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    LINER/CASING AROUND THE TAMPON ITSELF IS SEPARATING FROM THE TAMPON...THIS THIN LINER STICKS INSIDE AND HAS TO BE TORN AWAY FROM THE BODY [FOREIGN BODY IN REPRODUCTIVE TRACT]. UNCOMFORTABLE- VAGINAL [VULVOVAGINAL DISCOMFORT]. DISCOMFORT- INSIDE AROUND THE TAMPON [MEDICAL DEVICE SITE DISCOMFORT]. PAINFUL- VAGINAL [VULVOVAGINAL PAIN]. PAIN - INSIDE AROUND THE TAMPON [MEDICAL DEVICE SITE PAIN]. LINER/CASING AROUND THE TAMPON ITSELF IS SEPARATING FROM THE TAMPON [DEVICE BREAKAGE]. THE REMOVAL IS VERY PAINFUL [COMPLICATION OF DEVICE REMOVAL]. CASE NARRATIVE: CONSUMER REPORTED VIA E-MAIL THAT THE LINER/CASING AROUND THE TAMPON IS SEPARATING FROM THE TAMPON ITSELF. NO SERIOUS INJURY REPORTED.

    Patient problems: Discomfort; Foreign Body In Patient; Pain

    MAUDE report 22213287 ↗

Other Tampon, menstrual, unscented devices

All Tampon, menstrual, unscented devices →

Sources and updates

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