Waldemar Link GmbH & Co. KG (Mfg Site) recalls LinkSymphoKnee System

Some modular LinkSymphoKnee TiNbN Tibial Components were manufactured with two uncoated security screws, which is incorrect.

Waldemar Link notified consignees on about 07/31/2025 via URGENT: MEDCICAL DEVICE RECALL letter. Consignees were instructed to identify any affected units and arranging for their return to LinkBio Corporation, and to also complete and return the response form.

• FDA enforcement recordOfficial FDA database entry for Z-2541-2025
• FDA 510(k) clearance · K202924The device's official FDA premarket clearance record
• FDA device classification · JWHOfficial FDA classification for this device type
• CFR regulation · 21 CFR 888.3560The federal regulation governing this device
• FDA recall announcementSearch FDA.gov for the official press announcement
• Find Waldemar Link GmbH & Co. KG (Mfg Site)Search 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.