AllClear
PricingSign in
FDAJuly 14, 2016device

MicroVue BAP EIA, Model 8012, provides a quantitative measure of bone-specific alkaline phosphatase (BAP) activity in serum.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

There is a possibility of low volume and/or leaking standard bottles.

What to do

FDA enforcement status: Terminated

Brands named

diagnostic hybridsdiagnostic

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

Own something like this?

AllClear screens your whole list against every CPSC, FDA, USDA and NHTSA recall — and tells you the day a new one names something you own.

Start free — 200 items, no card →