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Tampax Tampax Pearl (UDI 00073010711242)Recalls & reported problems

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

All models of Tampax (40)

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

Adverse event reports
3
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00073010711242), received between Feb 24, 2026 and Aug 24, 2026 — classified as 1 injury, 2 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: 1 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 1 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
  • Adverse Event Without Identified Device or Use Problem2

Patient problems

  • Foreign Body In Patient3
  • Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1
  • Pain1
  • Unspecified Tissue Injury1

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

  • InjuryAug 24, 2026Insufficient Device Problem Information

    Staph infection "[Staphylococcal infection]".A "[tampon]" piece ripped off inside my vagina ¿ I got some pieces out ¿ and went to the emergency room where they removed the remaining pieces of tampon "[Foreign body in reproductive tract]".When I tried to remove "[tampon]", a piece ripped off inside my vagina ¿ it was really hard to get out/hard to expel "[Complication of device removal]".Tampon was broken and ripped "[Device breakage]".Case Narrative: Consumer reported via phone that a "[Tampon]" piece ripped off inside her vagina during removal, she got some pieces out and went to the emergency room to have the remaining pieces of the tampon removed. No serious injury was reportedFollow up received on 19-Aug-2026: Product return was received on (b)(6) 2026. Product investigation results: No failure could be identified as a result of the Investigation. No serious injury was reported.

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

    MAUDE report 50406444 ↗
  • MalfunctionApr 13, 2026Adverse Event Without Identified Device or Use Problem; Insufficient Device Problem Information

    TAMPON GOT STUCK IN VAGINA [FOREIGN BODY IN REPRODUCTIVE TRACT]. STRETCH MYSELF VAGINA [VULVOVAGINAL INJURY]. HURT VAGINA [VULVOVAGINAL PAIN]. HURT TAKING TAMPON OUT [COMPLICATION OF DEVICE REMOVAL]. (TAMPON GOT STUCK IN VAGINA) AND WHEN I WENT TO PULL IT OUT. IT WAS ONLY THE STRING [DEVICE BREAKAGE]. CASE NARRATIVE: CONSUMER REPORTED VIA PHONE THAT THE TAMPON GOT STUCK IN HER VAGINA AND ONLY THE STRING CAME OUT. NO SERIOUS INJURY REPORTED.

    Patient problems: Foreign Body In Patient; Pain; Unspecified Tissue Injury

    MAUDE report 24860833 ↗
  • MalfunctionFeb 24, 2026Adverse Event Without Identified Device or Use Problem; Insufficient Device Problem Information

    STRING UNRAVELING AND DETACHING FROM TAMPON.MAKES IT DIFFICULT TO REMOVE THE TAMPON WHEN NECESSARY, VAGINA FOREIGN BODY IN REPRODUCTIVE TRACT. BOTTOM HALF OF THE STRING ON MY TAMPON SIMPLY UNRAVELING AND DETACHING FROM TAMPON DEVICE BREAKAGE STRING UNRAVELING AND DETACHING FROM TAMPON. MAKES IT DIFFICULT TO REMOVE THE TAMPON WHEN NECESSARY. VAGINA COMPLICATION OF DEVICE REMOVAL. CASE NARRATIVE: CONSUMER REPORTED VIA E-MAIL THAT THE BOTTOM HALF OF THE STRING UNRAVELS. NO SERIOUS INJURY REPORTED.

    Patient problems: Foreign Body In Patient

    MAUDE report 24429855 ↗

Other TAMPON, MENSTRUAL, UNSCENTED devices

All TAMPON, MENSTRUAL, UNSCENTED devices →

Sources and updates

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