Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Talon Grasping Device Recalled by US Endoscopy Group Inc Due to A wire component on the distal grasping assembly...
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
Talon Grasping Device, 160 cm, US endoscopy. Used for retrieval of foreign bodies, tissue specimens, stones or calculi in endoscopic procedures of the gastrointestinal tract.
Quantity: 1695 units
Why Was This Recalled?
A wire component on the distal grasping assembly of the device became detached..
Where Was This Sold?
This product was distributed to 42 states: AL, AZ, AR, CA, CO, CT, FL, GA, ID, IL, IN, IA, KY, LA, ME, MD, MA, MI, MN, MS, MO, MT, NV, NJ, NY, NC, ND, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, WV, WI, DC
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