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Seventh Generation Regular, no applicatorRecalls & reported problems

Seventh Generation, Inc. · Organic Cotton No Applicator Tampons, Regular · Class 2

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 00732913451005), received between Oct 5, 2018 and Oct 5, 2018 — classified as 1 malfunction.

The most frequently reported specific device problem is “Misassembled” (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

  • Misassembled1

Patient problems

  • No Known Impact Or Consequence To Patient1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionOct 5, 2018Misassembled; Misassembled

    ONE REGULAR, NON-APPLICATOR TAMPON IN THE BOX HAD A SUBTLE GREY MOTTLED LOOK TO THE END OF THE TAMPON. WHEN OPENED IT SMELLED LIKE MOLD.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 7939166 ↗

Other Tampon, Menstrual, Unscented devices

All Tampon, Menstrual, Unscented devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.