Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
MicroVue BAP EIA Recalled by Diagnostic Hybrids, Inc. Due to There is a possibility of low volume and/or...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Diagnostic Hybrids, Inc. directly.
Affected Products
MicroVue BAP EIA, Model 8012, provides a quantitative measure of bone-specific alkaline phosphatase (BAP) activity in serum.
Quantity: 1004
Why Was This Recalled?
There is a possibility of low volume and/or leaking standard bottles.
Where Was This Sold?
This product was distributed to 12 states: CA, CT, GA, IL, KY, MD, MA, MO, PA, TX, WA, WI
About Diagnostic Hybrids, Inc.
Diagnostic Hybrids, Inc. has 6 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report