GN ReSound NX7CIC-MPRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 05708296335466), received between Aug 12, 2026 and Aug 12, 2026 — 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 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.

• InjuryAug 12, 2026Patient Device Interaction Problem

  It is reported that on the (b)(6) 2026, an in-the-ear (ITE) device had entered the user's ear canal deeper than usual, although he was still able to remove it himself. However, the following day, the same event occurred, and the user was unable to remove the device on his own, requiring a visit to the hospital.The device was successfully removed at the hospital.No further follow up is available.

  Patient problems: Foreign Body In Patient

  MAUDE report 50223148 ↗