Stayfree 07024Recalls & reported problems
Edgewell Personal Care Brands, LLC · SF MAXI SUP WLESS HTA OC 24 · Class 1
All models of Stayfree (2)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
1 FDA recall record name this device's identifier, 1 still open.
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.
Recalls naming this device
- Dec 26, 2025Class IIOpen, Classified
Potential exposure of rodents and rodent activity in the distribution center.
Z-1182-2026 · Root cause: Storage · Recall details · FDA record ↗
Other Pads, menstrual, scented-deodorized devices
- Stayfree 07032Edgewell Personal Care Brands, LLC · Pads, menstrual, scented-deodorized1 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
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026 · each recall links to the FDA recall notice
- 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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