JAS Diagnostics Drew Scientific DREW 3-PAC Reagent Kit containing: 5L Diluent, 750 mL recall — FDA Z-2656-2017
May result in elevated platelet backgrounds during routine startup/background checks.
Overview of recall records associated with JAS Diagnostics Inc., including dates, categories and classifications where available.
Classification mix: Class II: 1.
May result in elevated platelet backgrounds during routine startup/background checks.
This page summarizes recall records in which the official source identifies JAS Diagnostics Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.