Medline DYNJAETC70SRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10888277724792), received between Jun 14, 2024 and Jun 14, 2024 — classified as 2 injuries.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (2 reports).

1 other recall cover devices cleared under the same FDA submission (K042683); 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. 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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryJun 14, 2024Insufficient Device Problem Information; Insufficient Device Problem Information

  THE CUSTOMER REPORTED THAT, "THE ITEM WAS FOUND TO BE FAULTY DURING USE ON A PATIENT. THE ITEM FELL APART WHILE BEING INSERTED INTO THE PATIENT".

  Patient problems: Insufficient Information

  MAUDE report 19537849 ↗
• InjuryJun 14, 2024Insufficient Device Problem Information; Insufficient Device Problem Information

  THE CUSTOMER REPORTED THAT, "THE ITEM WAS FOUND TO BE FAULTY DURING USE ON A PATIENT. THE ITEM FELL APART WHILE BEING INSERTED INTO THE PATIENT".

  Patient problems: Insufficient Information

  MAUDE report 19537671 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K042683. One submission often covers many models, so check the product and lot details in each record.

• Z-3172-2026 · Jul 31, 2026 · Open, Classified
  SunMed Tracheal Tube, Size 2.5; Model Number: 1-7333-25