FDA recall Z-0738-2020

Diagnostica Stago, Inc. · Class II · device

Product

STA SYSTEM CONROL N + P (ref. 00678)

Reason for recall

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.

Distribution

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

Key facts

Status
Terminated
Initiation date
2019-11-18
Report date
2020-01-01
Termination date
2023-01-12
Voluntary/Mandated
Voluntary: Firm initiated
Location
Parsippany, NJ, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0738-2020