Tampax Tampax Pearl (UDI 00073010713383)Recalls & reported problems
Procter & Gamble Manufacturing Company, The · TAMPAX PEARL MULTI Super, Super Plus, Ultra · 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
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00073010713383), received between Aug 27, 2024 and Jul 16, 2025 — classified as 3 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
Most reported problems
Device problems
- Insufficient Device Problem Information2
- Adverse Event Without Identified Device or Use Problem1
- No Apparent Adverse Event1
Patient problems
- Abdominal Cramps1
- Cramp(s) /Muscle Spasm(s)1
- Foreign Body In Patient1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 16, 2025No Apparent Adverse Event; No Apparent Adverse Event
TAMPONS ARE COMPLETELY FALLEN APART [DEVICE BREAKAGE]. LEAVING PIECES WHERE THEY SHOULDN'T BE- TAMPON [PRODUCT RESIDUE PRESENT]. CASE NARRATIVE: CONSUMER REPORTED VIA E-MAIL THAT THE TAMPON HAS FALLEN APART. NO INJURY REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22518423 ↗MalfunctionMay 23, 2025Adverse Event Without Identified Device or Use Problem; Insufficient Device Problem Information; Adverse Event Without Identified Device or Use Problem; Insufficient Device Problem Information
RIPPED INSIDE ME...HAD TO DIG OUT PIECES OF THE TAMPON [FOREIGN BODY IN REPRODUCTIVE TRACT]. TAMPON RIPPED INSIDE ME- TAMPAX [DEVICE BREAKAGE]. CASE NARRATIVE: CONSUMER REPORTED VIA EMAIL THAT THE TAMPON RIPPED INSIDE OF HER. NO SERIOUS INJURY WAS REPORTED.
Patient problems: Foreign Body In Patient
MAUDE report 22077525 ↗MalfunctionAug 27, 2024Insufficient Device Problem Information; Insufficient Device Problem Information
CRAMPS STOMACH/(UTERUS AREA) [ABDOMINAL PAIN UPPER] . (CRAMPS STOMACH)/UTERUS AREA [UTERINE SPASM] . DEFECTIVE...SEEMS LIKE THE CORE IS UNRAVELING [DEVICE BREAKAGE] . LEAKING- TAMPONS [DEVICE INEFFECTIVE] . CASE NARRATIVE: CONSUMER REPORTED VIA PHONE THAT THE TAMPON CORE IS UNRAVELING. NO SERIOUS INJURY WAS REPORTED.
Patient problems: Abdominal Cramps; Cramp(s) /Muscle Spasm(s)
MAUDE report 20078289 ↗
Other TAMPON, MENSTRUAL, UNSCENTED devices
- U By Kotex KOTEX TAMPONSKimberly-Clark Global Sales, Inc. · Tampon, menstrual, unscented178 reports
- U By Kotex KOTEX TAMPONSKimberly-Clark Global Sales, Inc. · Tampon, menstrual, unscented126 reports
- U By Kotex KOTEX TAMPONSKimberly-Clark Global Sales, Inc. · Tampon, menstrual, unscented126 reports
- U by Kotex TamponKimberly-Clark Global Sales, Inc. · TAMPON, MENSTRUAL, UNSCENTED1 recall2 reports
- U by Kotex TamponKimberly-Clark Global Sales, Inc. · TAMPON, MENSTRUAL, UNSCENTED1 recall1 report
- U by Kotex TamponKimberly-Clark Global Sales, Inc. · TAMPON, MENSTRUAL, UNSCENTED1 recall0 reports
- Daye FG-TMP-REF00090009Tampon Innovations Ltd Ood · Tampon, Menstrual, Unscented1 recall0 reports
- Daye FG-TMP-RET00090009Tampon Innovations Ltd Ood · Tampon, Menstrual, Unscented1 recall0 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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