Seventh Generation Pad Maxi, OvernightRecalls & reported problems
Seventh Generation, Inc. · Maxi pad, Overnight · Class 1
Data updated Oct 16, 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 00732913450015), received between Jan 11, 2022 and Jan 11, 2022 — classified as 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Most reported problems
Device problems
- Device Contaminated During Manufacture or Shipping1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 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 13233794 ↗
Other Pad, Menstrual, Unscented devices
- Seventh Generation Pad Maxi, RegularSeventh Generation, Inc. · Pad, Menstrual, Unscented2 reports
- Carefree 07001Edgewell Personal Care Brands, LLC · Pad, menstrual, unscented1 report
- Seventh Generation Pad Ultrathin Super Long with WingsSeventh Generation, Inc. · Pad, Menstrual, Unscented1 report
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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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