[Recalled] ABL90 Flex Model #: 393-090 Portable, automated analyzer that measures pH, blood gases, electrolytes, glucose, lactate, bilirubin, and oximetry in whole blood. — Reports that the sample type "cord blood" has been changed int
This is an official product-safety recall record. Below are the verified details from the issuing authority, in plain language.
Recall details
| Product | ABL90 Flex Model #: 393-090 Portable, automated analyzer that measures pH, blood gases, electrolytes, glucose, lactate, bilirubin, and oximetry in whole blood. |
|---|---|
| Brand / manufacturer | Radiometer America Inc |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-1462-2017 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 26 January 2017 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Reports that the sample type "cord blood" has been changed into the two sample types "cord blood arterial" and "cord blood venous.
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 Radiometer America Inc
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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