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[Recalled] HemosIL Normal Control 1 UNASSAYED Part Number: 0020003120 — HemosIL Low, Abnormal, Normal Controls UNASSAYED (no-value assigned) lacks 510(… | FDA 2013-11-15

recall fda device united-states

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

Recall details

ProductHemosIL Normal Control 1 UNASSAYED Part Number: 0020003120
Brand / manufacturerInstrumentation Laboratory Co.
Categorydevice
Issuing authorityFDA_DEVICE
ReferenceZ-0514-2014
Country of noticeUnited States
Risk levelClass II
Hazard typerecall
Notice date15 November 2013
EAN / barcode0020003120

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.

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