Tampax Tampax Pearl (UDI 00073010479050)Recalls & reported problems
Procter & Gamble Manufacturing Company, The · TAMPAX PEARL SUPER PLUS 18CT · 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 00073010479050), received between Jan 9, 2025 and Feb 14, 2026 — classified as 4 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
- No Apparent Adverse Event2
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Foreign Body In Patient2
- No Clinical Signs, Symptoms or Conditions2
- Unspecified Infection1
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 14, 2026Insufficient Device Problem Information
INFECTION - VAGINAL [VAGINAL INFECTION]. LEFT PIECES OF THE COTTON AND STRING INSIDE ME; EMERGENCY ROOM FOUND 2 MORE LONG PIECES WAY UP INSIDE VAGINA [FOREIGN BODY IN REPRODUCTIVE TRACT]. FALLEN APART - TAMPAX [DEVICE BREAKAGE]. I'M REMOVING THE TAMPON. IT HAD FALLEN APART INSIDE MY VAGINA AND LEFT PIECES OF COTTON AND STRING INSIDE [COMPLICATION OF DEVICE REMOVAL]. CASE NARRATIVE: CONSUMER REPORTED VIA E-MAIL THAT THE TAMPON HAS FALLEN APART INSIDE HER. NO SERIOUS INJURY REPORTED.
Patient problems: Foreign Body In Patient; Unspecified Infection
MAUDE report 24340378 ↗MalfunctionJun 20, 2025No Apparent Adverse Event; No Apparent Adverse Event
SEVERAL LITTLE PIECES BROKE OFF THE SIDE- TAMPAX TAMPON [DEVICE BREAKAGE] CASE NARRATIVE: RELATIVE REPORTED VIA SOCIAL MEDIA THAT SEVERAL PIECES BROKE OFF THE TAMPON WHILE CONSUMER WAS REMOVING IT. NO INJURY WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22298417 ↗MalfunctionFeb 25, 2025No Apparent Adverse Event; No Apparent Adverse Event
STRINGS WERE ALREADY DETACHED OR JUST HANGING ON BY A THREAD- TAMPON [DEVICE PHYSICAL PROPERTY ISSUE]. PROBABLE MANUFACTURING CAUSE [MANUFACTURING ISSUE]. CASE NARRATIVE: CONSUMER REPORTED VIA E-MAIL THAT THE TAMPON STRINGS WERE ALREADY DETACHED OR HANGING ON BY A THREAD. NO INJURY REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21459816 ↗MalfunctionJan 9, 2025Adverse Event Without Identified Device or Use Problem; Insufficient Device Problem Information; Adverse Event Without Identified Device or Use Problem; Insufficient Device Problem Information
COTTON IS COMING APART INSIDE OF ME- VAGINA [FOREIGN BODY IN REPRODUCTIVE TRACT], COTTON IS COMING APART [DEVICE BREAKAGE] , WHEN I GO TO CHANGE MY TAMPON, THE COTTON IS COMING APART INSIDE OF ME [COMPLICATION OF DEVICE REMOVAL] . CASE NARRATIVE: CONSUMER REPORTED VIA E-MAIL THAT THE COTTON IS COMING APART INSIDE. NO SERIOUS INJURY REPORTED.
Patient problems: Foreign Body In Patient
MAUDE report 21111499 ↗
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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