Focus Diagnostics Inc: 5 recalls on record

Recalls filed with 1 agency: FDA (5).

First recall on record: November 7, 2012. Most recent: April 5, 2017.

Risk classification: Class II: 4 · Class III: 1

Most recent recalls

DateAgencyProduct
April 5, 2017FDALegionella IFA Substrate Slide (IF0951) intended for qualitatively detecting and semi-qua…Z-1686-2017
July 9, 2014FDASimplexa" Flu A/B & RSV Direct, Model Number: MOL2650. 510(k) K120413  Simplexa" F…Z-1958-2014
March 12, 2014FDASimplexa Flu AlB & RSV Direct Assay Kits, intended for use as an aid in the differential …Z-1144-2014
February 5, 2014FDASimplexa Flu A/B & RSV Direct assay, Model MOL2650. The Focus Diagnostics Simplexa Flu…Z-0846-2014
November 7, 2012FDAWest Nile Virus IgG DxSelect" kit Catalog No. EL0300G Kit Lots 122150, 122155, 122641, 1…Z-0182-2013

Questions about this company

How many recalls does Focus Diagnostics Inc have?
Recalert has 5 U.S. recalls on record for Focus Diagnostics Inc, published between November 7, 2012 and April 5, 2017.
What was the most recent Focus Diagnostics Inc recall?
FDA recall Z-1686-2017, published April 5, 2017: Legionella IFA Substrate Slide (IF0951) intended for qualitatively detecting and semi-quantitating human serum antibodies to Legionella pneumophila.
Which agencies have handled Focus Diagnostics Inc recalls?
Focus Diagnostics Inc appears as the recalling firm in recalls from: FDA (5).

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