ClearanceBrief
Recall Z-1514-2026 · KRO Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/Polymer

Waldemar Link GmbH & Co. KG (Mfg Site)

Endo-Model SL Connection Component incl. PE-Plateau; Item Number: 16-2840/07;

DateMar 10, 2026 (initiated Jan 12, 2026)
StatusOpen, Classified
ReasonThe potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.
Root causeUnder Investigation by firm
ActionOn or about January 12, 2026 URGENT FIELD SAFETY NOTICE Product Recall letters were sent to customers. Actions to be taken: Review inventory to identify and quarantine any affected product. Return any unused product to the manufacturer. Follow patient management recommendations, if implanted. A custom-made replacement set can be requested. If an affected product is noticed during implantation, another plateau screw from a replacement set or different LINK knee prosthesis package can be used. If this situation occurs, a complaint form must be completed and sent to Complaint@link-ortho.com. Th
Quantity31 units (OUS only)
DistributionWorldwide - US Nationwide distribution in the state of NJ and the countries of Belarus, Canada, Switzerland , Colombia, Germany, Spain, United Kingdom, Hungary, India, Italy, Netherlands, Romania, Saudi Arabia.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K151008LINK® MEGASYSTEM-C®
Waldemar Link GmbH & Co. KG, Aug 26, 2015