Tampax Tampax Pearl (UDI 00073010714410)Recalls & reported problems
Procter & Gamble Manufacturing Company, The · Tampax Pearl Ultra · 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 00073010714410), received between May 12, 2025 and May 4, 2026 — classified as 4 malfunctions.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (4 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 Information4
- Adverse Event Without Identified Device or Use Problem3
Patient problems
- Foreign Body In Patient4
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available2
- Abdominal Pain1
- Abnormal Vaginal Discharge1
- Anxiety1
- Discomfort1
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 4, 2026Insufficient Device Problem Information
TAMPON STUCK IN MY BACK END [FOREIGN BODY IN GASTROINTESTINAL TRACT]. TAMPON STUCK IN BACK END... HAVE COLON ISSUES... WAS RECOMMENDED TO USE THIS [INTENTIONAL DEVICE USE ISSUE]. TAMPON STUCK IN BACK END - RECTUM [INCORRECT ROUTE OF PRODUCT ADMINISTRATION]. CASE NARRATIVE: CONSUMER REPORTED VIA PHONE THAT THE TAMPON GOT STUCK IN HER BACK END. NO SERIOUS INJURY WAS REPORTED.
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available; Foreign Body In Patient
MAUDE report 25066902 ↗MalfunctionMar 20, 2026Adverse Event Without Identified Device or Use Problem; Insufficient Device Problem Information
(PIECES OF THE TAMPON ARE NOW RIPPING OFF) ...GETTING LEFT BEHIND- VAGINA [FOREIGN BODY IN REPRODUCTIVE TRACT]. PIECES OF THE TAMPON ARE NOW RIPPING OFF WHEN I PULL IT OUT AND GETTING LEFT BEHIND [COMPLICATION OF DEVICE REMOVAL]. PIECES OF THE TAMPON ARE NOW RIPPING OFF [DEVICE BREAKAGE]. CASE NARRATIVE: CONSUMER REPORTED VIA E-MAIL THAT PIECES OF THE TAMPON ARE RIPPING OFF. NO SERIOUS INJURY REPORTED.
Patient problems: Foreign Body In Patient
MAUDE report 24647914 ↗MalfunctionJan 30, 2026Adverse Event Without Identified Device or Use Problem; Insufficient Device Problem Information
CORE BROKE OFF INSIDE MY BODY- VAGINA [FOREIGN BODY IN REPRODUCTIVE TRACT] ODOR VAGINAL [VAGINAL ODOUR] ANXIETY [ANXIETY] PHYSICAL DISTRESS [ILL-DEFINED DISORDER] CORE BROKE OFF INSIDE MY BODY UPON ATTEMPTED REMOVAL- TAMPAX [COMPLICATION OF DEVICE REMOVAL] CORE BROKE OFF- TAMPON [DEVICE BREAKAGE] CASE NARRATIVE: CONSUMER REPORTED VIA E-MAIL THAT THE TAMPON CORE BROKE OFF UPON REMOVAL. NO SERIOUS INJURY WAS REPORTED.
Patient problems: Abnormal Vaginal Discharge; Anxiety; Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available; Foreign Body In Patient
MAUDE report 24222422 ↗MalfunctionMay 12, 2025Adverse Event Without Identified Device or Use Problem; Insufficient Device Problem Information; Adverse Event Without Identified Device or Use Problem; Insufficient Device Problem Information
PIECES OF THE TAMPON WERE FALLING OFF AND THEY HAD BEEN STUCK IN ME [FOREIGN BODY IN REPRODUCTIVE TRACT]. PAINFUL/LOWER ABDOMEN [ABDOMINAL PAIN LOWER]. DISCOMFORT- LOWER ABDOMEN [ABDOMINAL DISCOMFORT]. PIECES OF THE TAMPON WERE FALLING OFF [DEVICE BREAKAGE]. CASE NARRATIVE: CONSUMER REPORTED VIA PHONE THAT PIECES OF THE TAMPON WERE FALLING OFF AND BECAME STUCK IN HER. NO SERIOUS INJURY WAS REPORTED.
Patient problems: Abdominal Pain; Discomfort; Foreign Body In Patient
MAUDE report 22004172 ↗
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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