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OMNIlife science Inc. recalls OMNI K1 Broach Handle, Product Code HS-10054
Recalled February 20, 2019 · FDA recall Z-0837-2019 · OMNIlife science
Hazard
There is a potential for the inner pin of the handle to become loose and fall out. · FDA Class II
Units
7
Sold at
The products were distributed to the following US states: CA, GA, SC, and UT.
Description
There is a potential for the inner pin of the handle to become loose and fall out.
Product
OMNI K1 Broach Handle, Product Code HS-10054
Manufacturer(s)
OMNIlife science Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →