Medline DYNJAETC70Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10888277689565), received between Jul 13, 2023 and Sep 22, 2026 — classified as 1 injury, 1 malfunction.

The most frequently reported specific device problem is “Material Integrity Problem” (1 report).

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.

• MalfunctionSep 22, 2026Material Integrity Problem

  It was reported that "THE TIP IS TOO RIGID".

  Patient problems: Cramp(s) /Muscle Spasm(s); Hemorrhage/Blood Loss/Bleeding

  MAUDE report 50858625 ↗
• InjuryJul 13, 2023Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  ACCORDING TO THE FACILITY ON (B)(6) 2023 THE "TIP OF ENDOTRACHEAL TUBE PIERCED TONSIL WITHOUT SIGNIFICANT RESISTANCE, LEADING TO LACERATION AND FURTHER SURGERY".

  Patient problems: Hemorrhage/Blood Loss/Bleeding

  MAUDE report 17315246 ↗

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