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Seventh Generation Pad Maxi, RegularRecalls & reported problems

Seventh Generation, Inc. · Maxi Pad, Regular · Class 1

Adverse event reports
2
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00732913450008), received between Aug 10, 2021 and Jan 11, 2022 — classified as 1 injury, 1 malfunction.

The most frequently reported specific device problem is “Device Contaminated During Manufacture or Shipping” (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

  • Adverse Event Without Identified Device or Use Problem1
  • Device Contaminated During Manufacture or Shipping1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1
  • Rash1

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • MalfunctionJan 11, 2022Device Contaminated During Manufacture or Shipping; Device Contaminated During Manufacture or Shipping

    CONSUMER FOUND FOREIGN OBJECT IN MENSTRUAL PAD.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 13233737 ↗
  • InjuryAug 10, 2021Adverse Event Without Identified Device or Use Problem

    CONSUMER USED OUR REGULAR MAXI TAMPON. AFTER USE SHE NOTICED SKIN IRRITATION ONLY IN AREAS WHERE ADHESIVE CAME IN DIRECT CONTACT WITH SKIN AFTER MOVEMENT OF THE PAD. CONSUMER DISCONTINUED USING PRODUCT AND NO MEDICAL TREATMENT WAS SOUGHT.

    Patient problems: Rash

    MAUDE report 12302228 ↗

Other Pad, Menstrual, Unscented devices

All Pad, Menstrual, Unscented devices →

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