Diagnostic Hybrids MicroVue BAP EIA, Model 8012, provides a quantitative measure of recall — FDA Z-1797-2018
There is a possibility of low volume and/or leaking standard bottles.
Overview of recall records associated with Diagnostic Hybrids, Inc., including dates, categories and classifications where available.
Classification mix: Class II: 1.
There is a possibility of low volume and/or leaking standard bottles.
This page summarizes recall records in which the official source identifies Diagnostic Hybrids, 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.