Broselow 7700YINRecalls & reported problems
Carefusion Corporation · Broselow™ /Hinkle Pediatric Emergency System Yellow Intubation Module · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- 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 10885403423567), received between Jun 21, 2023 and Jun 21, 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. What reports can and can't tell you · How this data works · Data updated Oct 18, 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 21, 2023Patient-Device Incompatibility; Patient-Device Incompatibility
IT WAS REPORTED TO VYAIRE MEDICAL THAT THE BROSELOW YELLOW 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 17172588 ↗
Other Emergency response safety kit devices
- BROSELOW™ 7700REAAirlife · Emergency Response Safety Kit2 recalls0 reports
- BROSELOW™ 7730IALSAirlife · Emergency Response Safety Kit1 recall0 reports
- BROSELOW™ 7700REAirlife · Emergency Response Safety Kit1 recall0 reports
- BROSELOW™ 7730ALSAirlife · Emergency Response Safety Kit1 recall0 reports
- Broselow 7700WINCarefusion Corporation · Emergency response safety kit2 reports
- BROSELOW™ 7700PINVyaire Medical, Inc. · Emergency response safety kit1 report
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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