[Recalled] Recalled product is a component of the Newport Medical Instruments e360 Ventilator: single board computer, part number SBC2105A. Intended to provide invasive or noninvasive ventilator support and monitoring for infant, pediat
Authorities recorded a safety problem with this product. The details below come directly from the government recall notice.
Recall details
| Product | Recalled product is a component of the Newport Medical Instruments e360 Ventilator: single board computer, part number SBC2105A. Intended to provide invasive or noninvasive ventilator support and monitoring for infant, pediatric, and adult patients with respiratory failure or respiratory insuffi |
|---|---|
| Brand / manufacturer | Nellcor Puritan Bennett Inc. (dba Covidien LP) |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-1577-2014 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 18 April 2014 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Reports of the audible alarm not sounding when the ventilator is in an alarm state. The ventilator, as well as the visual and remote alarms, continue to operate normally.
This Class II recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Check whether your unit is affected and follow the authority's guidance before further use.
Read the full official notice →
Related recalls from Nellcor Puritan Bennett Inc. (dba Covidien LP)
This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.
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