Bock, Otto, Orthopedic Ind, Inc Modular Knee Joint with Friction Brake Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Modular Knee Joint with Friction Brake
Brand
Bock, Otto, Orthopedic Ind, Inc
Lot Codes / Batch Numbers
2004 and July 9, 2004.
Products Sold
No lot numbers are used. Recall covers patients who were fit with either of the products between March 1, 2004 and July 9, 2004.
Bock, Otto, Orthopedic Ind, Inc is recalling Modular Knee Joint with Friction Brake due to Braking Plates of the 3R90 and 3R92 Modular Knee Joint with Friction Brake may become dislodged which may cause the braking performance of the knee to. Based on FDA medical device recall database.
Summary derived from FDA notice
The following details were not provided by the FDA: distribution information.
Reason for Recall
As stated by FDA
Braking Plates of the 3R90 and 3R92 Modular Knee Joint with Friction Brake may become dislodged which may cause the braking performance of the knee to malfunction.
Recommended Action
Per FDA guidance
The braking plate of the knee may become dislodged, which may cause the braking performance of the knee to malfunction.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026