[Recalled] HemosIL Normal Control 1 UNASSAYED Part Number: 0020003120 — HemosIL Low, Abnormal, Normal Controls UNASSAYED (no-value assigned) lacks 510(… | FDA 2013-11-15
The product on this page is subject to an official recall. We summarise the regulator's findings and the recommended action.
Recall details
| Product | HemosIL Normal Control 1 UNASSAYED Part Number: 0020003120 |
|---|---|
| Brand / manufacturer | Instrumentation Laboratory Co. |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-0514-2014 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 15 November 2013 |
| EAN / barcode | 0020003120 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: HemosIL Low, Abnormal, Normal Controls UNASSAYED (no-value assigned) lacks 510(k) approval
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 Instrumentation Laboratory Co.
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.