Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
OMNI K1 Broach Handle Recalled by OMNIlife science Inc. Due to There is a potential for the inner pin...
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 OMNIlife science Inc. directly.
Affected Products
OMNI K1 Broach Handle, Product Code HS-10054
Quantity: 7
Why Was This Recalled?
There is a potential for the inner pin of the handle to become loose and fall out.
Where Was This Sold?
This product was distributed to 4 states: CA, GA, SC, UT
About OMNIlife science Inc.
OMNIlife science Inc. has 11 total recalls tracked by RecallDetector.
Related Recalls
EndoVive Safety PEG Kit Recalled by Boston Scientific Corporation Due to Recall of kits which utilized ChloraPrep Triple Swabsticks...
Boston Scientific Corporation · February 10, 2026
Owner's Booklets and Instructions for Use that are used with Recalled by Trividia Health, Inc. Due to The system labeling (user manual and online labeling)...
Trividia Health, Inc. · February 6, 2026
Artelon FlexBand Dynamic Matrix Ref: 31057 Recalled by International Life Sciences Due to Augmentation devices failed bacterial endotoxin testing.
International Life Sciences · February 6, 2026
Owner's Booklets and Instructions for Use that are used with Recalled by Trividia Health, Inc. Due to The system labeling (user manual and online labeling)...
Trividia Health, Inc. · February 6, 2026
Owner's Booklets and Instructions for Use that are used with Recalled by Trividia Health, Inc. Due to The system labeling (user manual and online labeling)...
Trividia Health, Inc. · February 6, 2026
Data sourced from the FDA (Device). Last updated March 26, 2026. View original report