AIR-FLOWRecalls & reported problems across all models
E.M.S. Electro Medical Systems S.A. · 2 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
3 open recalls name at least one AIR-FLOW 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
- 3
We found 2 models of AIR-FLOW by E.M.S. Electro Medical Systems S.A. in the FDA's device registry (GUDID). None of them is named in an adverse event report in our data.
3 FDA recall records name at least one of these models by its device identifier, 3 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
AIR-FLOW 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.
- Mar 13, 2024Open, Classified
Received complaints that bottles assembled with one batch of bottle collars can be disassembled in two parts when used under pressure (during treatment or storage if the use is not releasing the pressure inside the bottles).
Z-1688-2024 · Root cause: Process control · names 2 of these models · Recall details · FDA record ↗
- Mar 13, 2024Open, Classified
Received complaints that bottles assembled with one batch of bottle collars can be disassembled in two parts when used under pressure (during treatment or storage if the use is not releasing the pressure inside the bottles).
Z-1687-2024 · Root cause: Process control · names 2 of these models · Recall details · FDA record ↗
- Mar 13, 2024Open, Classified
Received complaints that bottles assembled with one batch of bottle collars can be disassembled in two parts when used under pressure (during treatment or storage if the use is not releasing the pressure inside the bottles).
Z-1686-2024 · Root cause: Process control · names 2 of these models · Recall details · FDA record ↗
AIR-FLOW models
2 models, most reported first. Each model has its own page with its reports, recalls and device details.
- AIR-FLOW FT-230HF-0B-302Airbrush3 recalls0 reports
- AIR-FLOW FT-230-2B-302Scaler, Ultrasonic3 recalls0 reports
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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