BROSELOWRecalls & reported problems across all models
Airlife · 4 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
5 open recalls name at least one BROSELOW model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls
- 5
We found 4 models of BROSELOW by Airlife in the FDA's device registry (GUDID). None of them is named in an adverse event report in our data.
5 FDA recall records name at least one of these models by its device identifier, 5 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. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
BROSELOW recalls
FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.
- Dec 15, 2025Open, Classified
Product contains potentially harmful dosing errors for Vecuronium, Flumazenil, and Ketamine.
Z-1117-2026 · Root cause: Device Design · Recall details · FDA record ↗
- 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 ↗
- Dec 15, 2025Open, Classified
Product contains potentially harmful dosing errors for Vecuronium, Flumazenil, and Ketamine.
Z-1115-2026 · Root cause: Device Design · Recall details · FDA record ↗
- Dec 15, 2025Open, Classified
Product contains potentially harmful dosing errors for Vecuronium, Flumazenil, and Ketamine.
Z-1114-2026 · Root cause: Device Design · Recall details · FDA record ↗
- May 15, 2025Open, Classified
The impacted tape was manufactured with incorrect information on the tape. Incorrect values are printed in the Red zone, Orange zone, and Grey zone. Using the incorrect values in the Red zone could lead to shocking a patient with an excessive dose of joules, causing significant harm including burns, heart damage, and cardiac arrest. Incorrect values in the Orange zone could lead to overdosing the patient with sodium bicarbonate and cause metabolic alkalosis, electrolyte imbalances, tissue damage, and worsen respiratory status. Incorrect information in the Grey may lead to underdosing the patient with sodium bicarbonate and may cause reduced myocardial contractility, decreased response to vasopressors, and increased risk of dysrhythmia.
Z-1904-2025 · Root cause: Process control · Recall details · FDA record ↗
BROSELOW models
4 models, most reported first. Each model has its own page with its reports, recalls and device details.
- BROSELOW™ 7700REAEmergency Response Safety Kit2 recalls0 reports
- BROSELOW™ 7700REEmergency Response Safety Kit1 recall0 reports
- BROSELOW™ 7730ALSEmergency Response Safety Kit1 recall0 reports
- BROSELOW™ 7730IALSEmergency Response Safety Kit1 recall0 reports
Other Airlife products
All Airlife devices →Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- 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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