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[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

recall fda device united-kingdom

The product on this page is subject to an official recall. We summarise the regulator's findings and the recommended action.

Recall details

ProductSpaceLabs Arkon Anesthesia Delivery System with Version 2.0 Software installed. This system includes a ventilator.
Brand / manufacturerDel Mar Reynolds Medical, Ltd.
Categorydevice
Issuing authorityFDA_DEVICE
ReferenceZ-1442-2014
Country of noticeUnited Kingdom
Risk levelClass I
Hazard typerecall
Notice date10 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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