BROSELOW™ 7730ALSRecalls & reported problems
Airlife · Broselow Domestic Complete ALS Organizer · Class 2
All models of BROSELOW (4)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
1 FDA recall record name this device's identifier, 1 still open.
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.
Recalls naming this device
- Dec 15, 2025Open, Classified
Product contains potentially harmful dosing errors for Vecuronium, Flumazenil, and Ketamine.
Z-1116-2026 · Root cause: Device Design · Recall details · FDA record ↗
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 7700WINCarefusion Corporation · Emergency response safety kit2 reports
- Broselow 7700YINCarefusion Corporation · Emergency response safety kit1 report
- 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
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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