Medline Industries, Inc. DYNJAANC40Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10080196503964), received between Oct 21, 2025 and Oct 21, 2025 — classified as 1 injury.

The most frequently reported specific device problem is “Connection 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 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryOct 21, 2025Connection Problem; Premature Separation; Connection Problem; Premature Separation

  ACCORDING TO THE FACILITY, "I ENCOUNTERED PREMATURE SEPARATION OF A NASOTRACHEAL TUBE FROM ITS CONNECTOR. THE EVENT WAS IMMEDIATELY RECOGNIZED WHEN END-TIDAL CO2 ABRUPTLY DROPPED TO ZERO. BECAUSE OF THE PROMPT ACTIONS, OXYGEN SATURATION REMAINED > 97%, AND THE TUBE WAS RECONNECTED, PREVENTING PATIENT HARM."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23353522 ↗

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