Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

US Endoscopy Padlock Clip defect closure system Ref: C910001 The Recalled by US Endoscopy Group Inc Due to Potential esophageal laceration during a patient procedure

Date: February 4, 2019
Company: US Endoscopy Group Inc
Status: Terminated
Source: FDA (Device)

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

US Endoscopy Padlock Clip defect closure system Ref: C910001 The Padlock Clip is indicated for use in flexible endoscopy and for the compression of tissue in the gastrointestinal tract, for hemostasis or for treating lesions of the wall of the gastrointestinal organs.

Quantity: 483 units ( 325 units US and 158 OUS)

Why Was This Recalled?

Potential esophageal laceration during a patient procedure

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About US Endoscopy Group Inc

US Endoscopy Group Inc has 10 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report