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
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
- 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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