Medline DYNJAETC75Recalls & reported problems

Summary

The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 10888277689572), received between Jul 29, 2019 and Sep 23, 2026 — classified as 2 injuries, 3 malfunctions.

The most frequently reported specific device problem is “Fitting 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 18, 2026.

Most reported problems

Recent adverse event reports

The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 23, 2026Loose or Intermittent Connection; Fitting Problem

  It was reported that "1 box of DYNJAETC75 under LOT 59224061677 is having difficulty with its connector component" and "the connector component is loose and cannot connect properly to the tube component."

  Patient problems: Laceration(s)

  MAUDE report 50871399 ↗
• InjuryMar 28, 2025Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  ACCORDING TO THE FACILITY ON (B)(6) 2025 "PATIENT WAS INTUBATED SUCCESSFULLY WITH 7.5 ET TUBE, THE HUB/PORT AT END OF TUBE THAT HAS THE STANDARD HARD PLASTIC PIECE THAT CONNECTS TO AMBU BAG OR VENTILATOR CIRCUIT POPPED OUT JUST AFTER INTUBATION WHEN CONNECTING THE AMBU BAG TO VENTILATE".

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

  MAUDE report 21724220 ↗
• MalfunctionDec 26, 2023Poor Visibility; Poor Visibility

  ET TUBE IS NOT SHOWING UP ON X-RAYS.

  Patient problems: Insufficient Information

  MAUDE report 18395451 ↗
• InjuryNov 28, 2023Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  ACCORDING TO THE FACILITY ON 10/21/23 THE PATIENT NEEDED TO BE REINTUBATED AS THE ENDOTRACHEAL TUBE WAS NOTED TO HAVE A LEAK AND THE CUFF WAS UNABLE TO RETAIN AIR.

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

  MAUDE report 18218504 ↗
• MalfunctionJul 29, 2019Gas/Air Leak

  IT WAS REPORTED THAT WHEN THE ENDOTRACHEAL TUBE WAS CONNECTED TO THE ANESTHESIA MACHINE, AIR INSIDE THE ENDOTRACHEAL TUBE'S BALLOON WAS LOST. THE PATIENT WAS EXTUBATED AND A NEW ENDOTRACHEAL TUBE WAS INSERTED.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 8839219 ↗

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