Class II

Medical Device Recall: Suture Cinch Long 1pk. Endoscopic tissue approximation device.

Boston Scientific Corporation · July 14, 2026

Reason for Recall

Device may fail to deploy the cinch implant and/or fail to cut the suture as intended.

Distribution

Worldwide distribution - US Nationwide and the countries of Austria, Azerbaijan, Belgium, Bulgaria, Canada, Chile, Costa Rica, Croatia, Czech Republic, Denmark, Dominican Republic, Egypt, Finland, France, Germany, Greece, Hong Kong, Hungary, Ireland, Israel, Italy, Japan, Latvia, Malta, Netherlands, Norway, Pakistan, Poland, Portugal, Qatar, Romania, Russian Federation, Saudi Arabia, Serbia, Slovakia, Spain, Sweden, Switzerland, Taiwan, Thailand, UAE, United Kingdom.

States Affected

NATIONWIDE

Quantity Affected

60,654 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2962-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.