OMNIlife science Inc. recalls OMNI K1 Broach Handle, Product Code HS-10054
- Recall date
- November 29, 2018
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-0837-2019
- FDA classification
- Class II
- Brand / firm
- OMNIlife science Inc.
- Sold / distributed
- The products were distributed to the following US states: CA, GA, SC, and UT.
Why it was recalled
There is a potential for the inner pin of the handle to become loose and fall out.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
OMNI K1 Broach Handle, Product Code HS-10054
Get recall alerts
Free email alert whenever OMNIlife science Inc. has a new recall — straight from official government data. Unsubscribe anytime.
More recalls from: OMNIlife science Inc.