[Recalled] IRISpec" CA/CB two-part urine chemistry control twin set, Iris Diagnostics part number 800-0074. Intended Use: IRISpec CA/CB is an assayed QC material for monitoring of the urine chemistry analytes and devices as listed on th
The product on this page is subject to an official recall. We summarise the regulator's findings and the recommended action.
Recall details
| Product | IRISpec" CA/CB two-part urine chemistry control twin set, Iris Diagnostics part number 800-0074. Intended Use: IRISpec CA/CB is an assayed QC material for monitoring of the urine chemistry analytes and devices as listed on the package insert. For in vitro diagnostic (IVD) use only. |
|---|---|
| Brand / manufacturer | Iris Diagnostics |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-2124-2012 |
| Country of notice | United States |
| Risk level | Class III |
| Hazard type | recall |
| Notice date | 09 July 2012 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: The firm recalled after it received complaints of IRISpec CA/CB two part Urine Chemistry Control, 101131-12, where the nitrite results read negative for the part B control, which should be positive.
This Class III 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 →
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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