Repair-It 1Recalls & reported problems
Majestic Drug CO. Inc. · Repair-It Advanced Denture Repair Kit repairs broken dentures and denture teeth in minutes: Fix breaks, replace loose teeth, and mend cracks. · Class 2
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 00010705400913), received between Apr 7, 2017 and Apr 7, 2017 — classified as 1 malfunction.
The most frequently reported specific device problem is “Missing Value Reason” (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
- Missing Value Reason1
Patient problems
- Patient Problem/Medical Problem1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 7, 2017Missing Value Reason; Missing Value Reason
THE PRODUCT IS AN OTC DENTURE REPAIR KIT. THE CUSTOMER STATED THAT SHE USED THE PRODUCT AND GOT SORES IN HER MOUTH. SHE WAS UNABLE TO EAT OR WEAR DENTURES. AS A RESULT SHE WENT TO THE EMERGENCY ROOM (ER). THE PATIENT WAS PRESCRIBED ANTIBIOTICS AND TOLD TO USE MOUTHWASH. THE CUSTOMER WAS TO FOLLOW-UP WITH A PRIVATE PHYSICIAN 1-2 DAYS AFTER. THE CUSTOMER HAD USED THE PRODUCT PREVIOUSLY WITH NO ADVERSE REACTION. FOLLOW-UP CALLS WERE PLACED BY COMPANY CUSTOMER SERVICE WITH NO ANSWER.
Patient problems: Patient Problem/Medical Problem
MAUDE report 6471501 ↗
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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