[Recalled] SpaceLabs Arkon Anesthesia Delivery System with Version 2.0 Software installed. This system includes a ventilator. — The System may go into a controlled failed state if a series of parameters on t… | FDA 2014-03-10
The product on this page is subject to an official recall. We summarise the regulator's findings and the recommended action.
Recall details
| Product | SpaceLabs Arkon Anesthesia Delivery System with Version 2.0 Software installed. This system includes a ventilator. |
|---|---|
| Brand / manufacturer | Del Mar Reynolds Medical, Ltd. |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-1442-2014 |
| Country of notice | United Kingdom |
| Risk level | Class I |
| Hazard type | recall |
| Notice date | 10 March 2014 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: The System may go into a controlled failed state if a series of parameters on the user interface are activated in a specific sequence.
This Class I recall concerns device products distributed in United Kingdom 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
Stop using the product immediately and follow the authority's remedy (return, repair, or disposal).
Read the full official notice →
Related recalls from Del Mar Reynolds Medical, Ltd.
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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