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Diagnostic Hybrids, Inc. recalls MicroVue BAP EIA, Model 8012, provides a quantitative measure of bone-specific alkaline phosphatase (BAP) activity in se
Recalled May 16, 2018 · FDA recall Z-1797-2018 · Diagnostic Hybrids
Hazard
There is a possibility of low volume and/or leaking standard bottles. · FDA Class II
Units
1004
Sold at
The products were distributed to the following US states: CA, CT, GA, IL, KY, MA, MD, MO, PA, TX, WA, and WI. The products were distributed to the following foreign countries: Australia, Brazil, Canada, China, Costa Rica, India, Japan, Mexico, The Philippines, Russia, South Korea, South Africa, Switzerland, and Uruguay.
Description
There is a possibility of low volume and/or leaking standard bottles.
Product
MicroVue BAP EIA, Model 8012, provides a quantitative measure of bone-specific alkaline phosphatase (BAP) activity in serum.
Manufacturer(s)
Diagnostic Hybrids, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →