Carefree 07001Recalls & reported problems
Edgewell Personal Care Brands, LLC · CF Thong 49ct 9/cs · Class 1
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 00078300070016), received between Nov 29, 2018 and Nov 29, 2018 — classified as 1 injury.
The most frequently reported specific device problem is “Patient-Device Incompatibility” (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
- Patient-Device Incompatibility1
Patient problems
- Cellulitis1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryNov 29, 2018Patient-Device Incompatibility; Patient-Device Incompatibility
A (B)(6) YEAR OLD FEMALE CONSUMER REPORTED THAT BEGINNING IN (B)(6) 2018, EACH TIME SHE WOULD HAVE HER PERIOD SHE WOULD NOTICE AN IRRITATION IN HER PERINEAL AREA THAT WAS VERY PAINFUL. SHE STATED THAT SHE STARTED CHANGING THINGS BUT ONLY USED PANTY LINERS DURING MENSTRUATION, HAD USED THEM FOR YEARS AND DID NOT CHANGE BRANDS. SHE WENT TO HER DOCTOR AND WAS PRESCRIBED ANTIBIOTICS AND STATED THAT NOTHING WOULD HELP. SHE PURCHASED AN ANTI-ITCH CREAM TO TREAT THE REACTIONS THAT SHE STATED OCCURRED FOUR TIMES. CONSUMER STATED THAT SHE WENT TO HER PHYSICIAN'S OFFICE TWICE BEFORE BEING ADMITTED TO THE HOSPITAL ON (B)(6) 2018. SHE REPORTED THAT SHE WAS TESTED FOR SEXUALLY TRANSMITTED DISEASES (STDS) AND A COMPLETE BLOOD COUNT (CBC) WAS DONE AND ALL RESULTS WERE NEGATIVE. SHE STATED THAT SHE WAS THEN DIAGNOSED WITH A CELLULITIS SKIN INFECTION FROM THE OPEN SORES. DURING THE HOSPITALIZATION SHE WAS TREATED WITH NUMEROUS ANTIBIOTICS AND STEROIDS: VANCOMYCIN, KETOCONAZOLE, CLOTRIMAZOLE, AMITRIPTYLINE, TRIAMCINOLONE, DOXYCYCLINE AND HYDROXYZINE FOR ITCHING. THE CONSUMER REPORTED THAT SHE WAS IN THE HOSPITAL FOR FOUR NIGHTS AND WAS DISCHARGED FROM THE HOSPITAL OVER THE MEMORIAL DAY HOLIDAY WEEKE
Patient problems: Cellulitis
MAUDE report 8115766 ↗
Other Pad, menstrual, unscented devices
- Seventh Generation Pad Maxi, RegularSeventh Generation, Inc. · Pad, Menstrual, Unscented2 reports
- Seventh Generation Pad Maxi, OvernightSeventh Generation, Inc. · 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 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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