Chamberlain Technologies LLC recalls SURGIMESH WN

Potential presence of residual adhesive material on the mesh surface.

Customer notification began 8/12/22. Initial communication was made directly (by phone and in-person visit). This communication instructed users to segregate and return the affected product to BG Medical. If you have any questions, call 8473044069 or email: d.howard@surgimesh.com.

• FDA enforcement recordOfficial FDA database entry for Z-1986-2025
• FDA 510(k) clearance · K061445The device's official FDA premarket clearance record
• FDA device classification · FTLOfficial FDA classification for this device type
• CFR regulation · 21 CFR 878.3300The federal regulation governing this device
• FDA recall announcementSearch FDA.gov for the official press announcement
• Find Chamberlain Technologies LLCSearch for the manufacturer's official notice
• News coverageRecent reporting on this recall and manufacturer
• openFDA data recordThe raw JSON record this page is built from

Source: U.S. FDA openFDA device enforcement reports. This summary is informational and may lag or differ from the official record. Always verify against the FDA before acting.