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JAS Diagnostics/Drew Scientific

Country not established FDA establishment FEI 3003071743

Devices
0
Registrations
FDA
FDA recalls
1

No devices from this company are in the catalogue yet.

Company details

FDA FEI number
3003071743
Address
6600 NW 14th Street, Plantation, FL, 33313

FDA recalls1

Recalls are matched to the firm by name. FDA recall data as of 22 Oct 2026.

  • 2016

    • 10 Mar 2016 Z-1576-2016 Class II Terminated The reagent pack may result in elevated platelet background during Drew3 Hematology Analyzer routine check. Distribution: Worldwide Distribution - US Distribution including the states of : AL, AR, CA, FL, GA, IA, IN, KS, KY, LA, MA, MN, MO,…
      Full distribution text Worldwide Distribution - US Distribution including the states of : AL, AR, CA, FL, GA, IA, IN, KS, KY, LA, MA, MN, MO, MS, NC, NE, NY, SC, TN, and TX. and to the countries of : Bolivia, Cairo, Columbia, Ecuador, Italy, Moscow, Netherlands, Pakistan, Peru, Slovenia, Spain, and Venezuela.
      Submission number: K071562

This is an FDA establishment record without devices in deviCERTS.