Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Histolock Resection Device Recalled by US Endoscopy Group Inc Due to The company has determined the sterility cannot be...
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 US Endoscopy Group Inc directly.
Affected Products
Histolock Resection Device, US Endoscopy. An electrosurgical device designed to be used to endoscopically grasp, dissect and transect tissue during gastrointestinal endoscopic procedures.
Quantity: 41 units
Why Was This Recalled?
The company has determined the sterility cannot be assured for the affected lot.
Where Was This Sold?
This product was distributed to 9 states: AL, AR, CA, IL, IN, MS, OH, OK, TN
About US Endoscopy Group Inc
US Endoscopy Group Inc has 10 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report