Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Endoscopic retrieval device. The disposable Raptor grasping device in intended Recalled by US Endoscopy Group Inc Due to When the outer catheter is either coiled or...
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
Endoscopic retrieval device. The disposable Raptor grasping device in intended to retrieve foreign bodies or resected tissue specimens in endoscopic procedures of the upper and lower gastrointestinal tract or biliary tract.
Quantity: 1153
Why Was This Recalled?
When the outer catheter is either coiled or in a contorted configuration outside of the endoscope and the patient, and excessive force is applied to the handle, the jaws may become inoperable and may become stuck in the open condition.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
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