AMT Mini™ Extension Set E6-1221Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00842071107062), received between Feb 25, 2021 and Feb 25, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Break” (1 report).

1 other recall cover devices cleared under the same FDA submission (K110804, K123716, K945618); they may or may not involve this specific model.

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.

• MalfunctionFeb 25, 2021Break; Entrapment of Device

  PER THE ORIGINAL MEDWATCH REPORT RECEIVED WITH REFERENCE #: MW5098551: "PATIENT'S MOTHER CALLED TO SAY PORT CONNECTOR TO G PORT BROKE AND LODGED ITSELF INSIDE THE ORIFICE. ER VISIT WAS REQUIRED TO REMOVE THE BROKEN PIECE."

  Patient problems: Foreign Body In Patient

  MAUDE report 11380788 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K110804, K123716, K945618. One submission often covers many models, so check the product and lot details in each record.

• Z-1497-2016 · Jan 26, 2016 · Terminated
  AMT G-Jet Low-Profile Transgastric-Jejunal Feeding Device 14F 1.5cm 45cm SINGLE USE ONLY Rx ONLY STERILE. For use in patients who cannot absorb adequate nutrition through the stoma