Playtex 02603Recalls & reported problems
Edgewell Personal Care Brands, LLC · Playtex Sport 50ct MultiPack Tampons (Re/Super) · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00078300026037), received between Jun 15, 2020 and Jun 15, 2020 — classified as 1 injury.
The most frequently reported specific device problem is “Expulsion” (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. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Expulsion1
Patient problems
- Bacterial Infection1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJun 15, 2020Expulsion; Expulsion
A FEMALE CONSUMER, OVER THE AGE OF 18 YEARS, REPORTED THAT THE COTTON FROM THE TAMPON WAS COMING OFF INSIDE OF HER AND CAUSED HER TO GO TO THE HOSPITAL DUE TO AN INFECTION. WHEN THE CONSUMER WAS CONTACTED ON (B)(6) 2020 SHE REPORTED THAT SHE SOUGHT MEDICAL ATTENTION AT PLANNED PARENTHOOD ON (B)(6) 2020. SHE STATED THAT SHE WAS DIAGNOSED WITH BACTERIAL VAGINOSIS AND PRESCRIBED VAGINAL CREAM (NAME NOT PROVIDED). CONSUMER STATED THAT TESTS WERE PERFORMED BUT DID NOT PROVIDE THE TESTS OR RESULTS. AT THE TIME OF THIS REPORT NO ADDITIONAL FOLLOW UP WAS REQUIRED AND THE CONSUMER WAS RECOVERING.
Patient problems: Bacterial Infection
MAUDE report 10154766 ↗
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
- Daye FG-TMP-MM-IB18180000Tampon Innovations Ltd Ood · Tampon, Menstrual, Unscented1 recall0 reports
- Daye FG-TMP-RET09000900Tampon Innovations Ltd Ood · Tampon, Menstrual, Unscented1 recall0 reports
- Daye FG-TMP-MM-REF18180000Tampon 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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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