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
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
- 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.
How reports and recalls are matched · Editorial policy · Report an error on this page