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American Eagle Instruments AEGDP13-14XPXRecalls & reported problems

American Eagle Instruments, Inc. · Class 1

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 00841013107771), received between Jul 2, 2019 and Jul 2, 2019 — classified as 1 malfunction.

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. How this data works · Data updated Oct 13, 2026.

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.

  • MalfunctionJul 2, 2019Break

    CURETTE TIP BROKE OFF DURING ROOT CLEANING DISTOLINGUAL CORNER OF TOOTH 6- (1. MOLAR RIGHT LOWER JAW). DEEP POCKET 8 MM. TIP OF INSTRUMENT (~2.5 MM FROM END) BROKE OFF IN PATIENTS MOUTH DURING USE. THE PATIENT HAD TO UNDERGO SURGERY TO HAVE THE TIP REMOVED. THE TIP WAS SUCCESSFULLY REMOVED FROM THE PATIENT AND THE PATIENT MADE A FULL RECOVERY.

    Patient problems: Foreign Body In Patient

    MAUDE report 8753876 ↗

Other CURETTE, PERIODONTIC devices

All CURETTE, PERIODONTIC devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.