Tampax Tampax Radiant (UDI 00073010631090)Recalls & reported problems
Procter & Gamble Manufacturing Company, The · TAMPAX RADIANT MULTI REGULAR SUPER SUPER PLUS · Class 2
All models of Tampax (40)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00073010631090), received between Mar 24, 2026 and Mar 24, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (1 report).
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
- Adverse Event Without Identified Device or Use Problem1
- Insufficient Device Problem Information1
Patient problems
- Abdominal Pain1
- Abnormal Vaginal Discharge1
- Foreign Body In Patient1
- Malaise1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 24, 2026Adverse Event Without Identified Device or Use Problem; Insufficient Device Problem Information
I FOUND THREE PIECES OF TAMPON INSIDE ME- VAGINA [FOREIGN BODY IN REPRODUCTIVE TRACT] PAIN STOMACH, HURT MY STOMACH [ABDOMINAL PAIN UPPER] BODY FELT LIKE I WAS GETTING SICK ALL OVER [MALAISE] ODOR VAGINA, GAVE ME VERY BAD ODOR [VAGINAL ODOUR] BAD DISCHARGE VAGINA [VAGINAL DISCHARGE] THREE PIECES OF TAMPON (INSIDE ME)- TAMPON [DEVICE BREAKAGE] . CASE NARRATIVE: CONSUMER REPORTED VIA E-MAIL THAT SHE FOUND THREE PIECES OF TAMPON INSIDE HER. NO SERIOUS INJURY REPORTED.
Patient problems: Abdominal Pain; Abnormal Vaginal Discharge; Foreign Body In Patient; Malaise
MAUDE report 24673000 ↗
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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