AH PLUS JET 667005Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI D0106670051), received between Oct 19, 2023 and Oct 19, 2023 — classified as 1 injury.

The most frequently reported specific device problem is “Patient Device Interaction Problem” (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

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryOct 19, 2023Patient-Device Incompatibility; Patient Device Interaction Problem; Patient-Device Incompatibility; Patient Device Interaction Problem

  IN THIS EVENT IT IS REPORTED THAT AH PLUS JET START KIT MAIL.NA THAT WAS USED IN TREATMENT HAD A MALFUNCTION WITH THE AUTO MIXING TIP. THE UNMIXED SEALER WENT OUT OF THE APEX AND REPORTEDLY CAUSED A CHEMICAL BURN OF PATIENT'S MENTAL NERVE - RIGHT SIDE OF FACE. THE PATIENT REPORTEDLY DEVELOPED NUMBNESS IN THE RIGHT HALF OF THE CHIN AND LOWER LIP AND PAIN ON THE WHOLE RIGHT SIDE OF THEIR FACE TWO DAYS AFTER EXPOSURE TO AH PLUS JET DURING ROOT CANAL TREATMENT. THE SYMPTOMS ARE STILL ONGOING. THE DENTIST ALLEGES THIS WAS DUE TO AN ISSUE WITH THE AUTO-MIXING TIP, WHICH WOULD NOT HAVE MIXED THE PRODUCT CORRECTLY, IN TURN LEADING TO UNMIXED MATERIAL COMING INTO CONTACT WITH THE NERVE AND CAUSING A CHEMICAL BURN. CUSTOMER/DENTIST REPORTS THAT THIS WAS NOT AN ALLERGIC REACTION.

  Patient problems: Caustic/Chemical Burns; Hypersensitivity/Allergic reaction; Numbness

  MAUDE report 17967638 ↗