HU-FRIEDY XP23/NC127Recalls & reported problems
Hu-Friedy Mfg. CO., LLC · #23/UNC12 Expro, #7 Handle · Class 1
Data updated Oct 18, 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 10889950034931), received between Mar 26, 2026 and Mar 26, 2026 — classified as 1 injury.
The most frequently reported specific device problem is “Break” (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 18, 2026.
Reports received per month
Most reported problems
Device problems
- Break1
Patient problems
- Foreign Body In Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMar 26, 2026Break
THE USER FACILITY REPORTED THAT DURING A DENTAL PROCEDURE THE TIP OF THE PROBE BROKE IN PATIENT'S MOUTH AND THE PATIENT MIGHT HAVE SWALLOWED IT. A RADIOGRAPH WAS TAKEN TO LOCATE THE TIP AND THEY FOUND NO EVIDENCE OF THE TIP. PATIENT DECLINED ANY FURTHER MEDICAL INTERVENTION.
Patient problems: Foreign Body In Patient
MAUDE report 24702145 ↗
Other PROBE, PERIODONTIC devices
- American Eagle Instruments AEEP23/12BXAmerican Eagle Instruments, Inc. · PROBE, PERIODONTIC1 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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