[Recalled] ENVOY 500 AST Reagent Kit, reference Model/Catalog 55255, for Envoy 500. Intended Use of the Product: Envoy 500 AST Reagent is for the quantitative in vitro diagnostic determination of aspartate aminotransferase (AST) in hu
This is an official product-safety recall record. Below are the verified details from the issuing authority, in plain language.
Recall details
| Product | ENVOY 500 AST Reagent Kit, reference Model/Catalog 55255, for Envoy 500. Intended Use of the Product: Envoy 500 AST Reagent is for the quantitative in vitro diagnostic determination of aspartate aminotransferase (AST) in human serum and plasma using the Envoy 500 Chemistry System. Aspartate |
|---|---|
| Brand / manufacturer | ELITech Clinical Systems SAS |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-0006-2015 |
| Country of notice | France |
| Risk level | Class III |
| Hazard type | recall |
| Notice date | 11 August 2014 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Some users of ENVOY 500 AST Reagent Kit, reference 55255, for Envoy 500 systems are observing that Quality Control (QC) fails before the product expiry is reached.
This Class III recall concerns device products distributed in France 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 ELITech Clinical Systems SAS
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.