Medical device recalls Moderate risk

Diagnostica Stago, Inc. recalls STA SYSTEM CONROL N + P (ref. 00678)

Recall date
November 18, 2019
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-0738-2020
FDA classification
Class II
Brand / firm
Diagnostica Stago, Inc.
Sold / distributed
US: MA ME VT CT NJ NY PA DC MD VA NC SC GA FL AL TN MS KY OH IN MI IA WI MN SD ND MT IL MO KS LA AR OK TX CO AZ NV CA HI OR WA AK

Why it was recalled

A positive bias was confirmed to exists on the STA - Unicalibrator levels with STA - Deficient IX and STA - Deficient VIII when compared to the International Standard (IS) for factor VIII or IX. This bias is also observed on several External Quality Assessment (EQA) results.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

STA SYSTEM CONROL N + P (ref. 00678)

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