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BROSELOW™ 7700PINRecalls & reported problems

Vyaire Medical, Inc. · INTUBATION MODULES · Class 2

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10190752158016), received between Jun 19, 2023 and Jun 19, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Patient-Device Incompatibility” (1 report).

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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Patient-Device Incompatibility1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionJun 19, 2023Patient-Device Incompatibility; Patient-Device Incompatibility

    IT WAS REPORTED TO VYAIRE MEDICAL THAT THE BROSELOW PURPLE INTUBATION MODULE 2PK CONTAINS AN ADULT SIZE STYLET (10FR) THAT IS TOO BIG FOR THE PEDIATRIC ENDOTRACHEAL TUBES THAT CAN CAUSE A DEADLY OUTCOME. FURTHERMORE, THERE IS NO PATIENT ASSOCIATED WITH THE SAID EVENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 17153493 ↗

Other Emergency response safety kit devices

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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.