IncaRecalls & reported problems across all models
Coopersurgical, Inc. · 9 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
2 open recalls name at least one Inca 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
- 2
We found 9 models of Inca by Coopersurgical, Inc. in the FDA's device registry (GUDID). None of them is named in an adverse event report in our data.
2 FDA recall records name at least one of these models by its device identifier, 2 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
Inca 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.
- Aug 11, 2026Open, Classified
Potential to exhibit a loose connection between the flexible tubing and the nasal cannula, during assembly or while in use, which may result in loss of CPAP pressure, possibly reducing the effectiveness of treatment and lead to decreased oxygenation until connection is restored.
Z-3140-2026 · Root cause: Device Design · names 4 of these models · Recall details · FDA record ↗
- Aug 11, 2026Open, Classified
Potential to exhibit a loose connection between the flexible tubing and the nasal cannula, during assembly or while in use, which may result in loss of CPAP pressure, possibly reducing the effectiveness of treatment and lead to decreased oxygenation until connection is restored.
Z-3139-2026 · Root cause: Device Design · names 5 of these models · Recall details · FDA record ↗
Inca models
9 models, most reported first. Each model has its own page with its reports, recalls and device details.
- Inca 44-2707Ventilator, Non-Continuous (Respirator)1 recall0 reports
- Inca 44-2709Ventilator, Non-Continuous (Respirator)1 recall0 reports
- Inca 44-2710Ventilator, Non-Continuous (Respirator)1 recall0 reports
- Inca 44-2712Ventilator, Non-Continuous (Respirator)1 recall0 reports
- Inca 44-2715Ventilator, Non-Continuous (Respirator)1 recall0 reports
- Inca 44-0707Ventilator, Non-Continuous (Respirator)1 recall0 reports
- Inca 44-0709Ventilator, Non-Continuous (Respirator)1 recall0 reports
- Inca 44-0712Ventilator, Non-Continuous (Respirator)1 recall0 reports
- Inca 44-0715Ventilator, Non-Continuous (Respirator)1 recall0 reports
Other Coopersurgical, Inc. products
All Coopersurgical, Inc. 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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