Diagnostic Hybrids recalls

Diagnostic Hybrids appears in 8 official U.S. recall notices indexed by RecallRadar, most recently on 2018-05-16.

Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.

• MicroVue BAP EIA, Model 8012, provides a quantitative measure of bone-specific alkaline phosphatase (BAP) activity in serum
  FDA Device · Class II · 2018-05-16 · Diagnostic Hybrids
• MicroVue SC5b-9 Plus EIA (RUO), Model A020
  FDA Device · Class III · 2018-05-02 · Diagnostic Hybrids
• MicroVue CIC-C1q EIA, Model A001
  FDA Device · Class II · 2018-05-02 · Diagnostic Hybrids
• Quidel MicroVue Intact PTH EIA, Model 8044
  FDA Device · Class III · 2018-05-02 · Diagnostic Hybrids
• MicroVue CIC-C1q EIA, Model A001
  FDA Device · Class III · 2018-05-02 · Diagnostic Hybrids
• MicroVue SC5b-9 Plus EIA (CE-IVD), Model A029
  FDA Device · Class III · 2018-05-02 · Diagnostic Hybrids
• MicroVue Bb Plus EIA is packaged as a kit which contains all reagent components to perform the test
  FDA Device · Class II · 2015-09-09 · Diagnostic Hybrids
• Diagnostic Hybrids, Inc., RhMK, Model #:49-0600, 49-0600A, 49-0102A, and 49-T075A. Culture media, used in the cultivation and amplification…
  FDA Device · Class III · 2013-02-13 · Diagnostic Hybrids