Medline DYNJAETC30Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10888277689480), received between Jun 2, 2023 and Apr 10, 2025 — classified as 2 injuries.

The most frequently reported specific device problem is “Inadequacy of Device Shape and/or Size” (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.

• InjuryApr 10, 2025Accessory Incompatible; Material Too Rigid or Stiff; Inadequacy of Device Shape and/or Size

  PER SEVERAL PHYSICIANS OF OUR ORGANIZATION, FROM BOTH ANESTHESIA AND OTOLARYNGOLOGY, THERE ARE CONCERNS OF THIS ENDOTRACHEAL TUBE HAVING A "RIGID" FEELING TIP WITH A MASSIVE CUFF. THE INTERNAL SIZE IS TOO NARROW TO ALLOW THE BRONCHOSCOPE THROUGH AND HAS BEEN TOO WIDE AND STIFF TO ALLOW FOR SUCCESSFUL INTUBATION. ONE PATIENT INVOLVED WAS ADMITTED TO CTICU(CARDIOTHORACIC INTENSIVE CARE UNIT) WITH AIRWAY TRAUMA. THERE ARE ALSO SEVERAL PATIENTS SCHEDULED FOR BRONCHOSCOPY TO EVALUATE THEIR AIRWAYS.

  Patient problems: Unspecified Tissue Injury

  MAUDE report 21814535 ↗
• InjuryJun 2, 2023Inadequacy of Device Shape and/or Size; Inadequacy of Device Shape and/or Size

  UNABLE TO REMOVE TUBE, LEADING TO ICU ADMISSION.

  Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available

  MAUDE report 17050321 ↗

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