OMNI K1 Broach Handle, Product Code HS-10054
Reported: February 20, 2019 Initiated: November 29, 2018 #Z-0837-2019
Product Description
OMNI K1 Broach Handle, Product Code HS-10054
Reason for Recall
There is a potential for the inner pin of the handle to become loose and fall out.
Details
- Recalling Firm
- OMNIlife science Inc.
- Units Affected
- 7
- Distribution
- The products were distributed to the following US states: CA, GA, SC, and UT.
- Location
- Raynham, MA
Frequently Asked Questions
What product was recalled? ▼
OMNI K1 Broach Handle, Product Code HS-10054. Recalled by OMNIlife science Inc.. Units affected: 7.
Why was this product recalled? ▼
There is a potential for the inner pin of the handle to become loose and fall out.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on February 20, 2019. Severity: Moderate. Recall number: Z-0837-2019.
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