[Recalled] Giraffe OmniBed with installed Servo Oxygen module. Infant incubator and warmer. — Potential for certain Giraffe Incubators and Giraffe OmniBeds to deliver a diff… | FDA 2020-04-28
The product on this page is subject to an official recall. We summarise the regulator's findings and the recommended action.
Recall details
| Product | Giraffe OmniBed with installed Servo Oxygen module. Infant incubator and warmer. |
|---|---|
| Brand / manufacturer | GE Healthcare, LLC |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-2235-2020 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 28 April 2020 |
| EAN / barcode | 66000849 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Potential for certain Giraffe Incubators and Giraffe OmniBeds to deliver a different environmental oxygen level than what is displayed by the device, if a certain optional component referred to as the Servo Oxygen Module is installed.
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 GE Healthcare, LLC
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.