Ossur H F Grjothals 5 Reykjavik Iceland Total Knee Junior Model Number 1100 Product Usage: The Total Knee Junior is an external polycentric prosthetic knee with a geometric locking system. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Total Knee Junior Model Number 1100 Product Usage: The Total Knee Junior is an external polycentric prosthetic knee with a geometric locking system.
Brand
Ossur H F Grjothals 5 Reykjavik Iceland
Lot Codes / Batch Numbers
Serial Numbers: 8573, 8574, 8575, 8577, 8578, 8580, 8581, 8582, 8583, 8584, 8585, 8586, 8587, 8588, 8589, 8599, 8600, 8602, 8603, 8604, 8605, 8606, 8609, 8610, 8611, 8613, 8616, 8620, 8621, 8622, 8624, 8628, 8629, 8630, 8631, 8632, 8633, 8634, 8635, 8636, 8638, 8639, 8640, 8642, 8643, 8644, 8645, 8646, 8666, 8670, 8671, 8672, 8673, 8674, 8675, 8678, 8679, 8680, 8682, 8684, 8685, 8687, 8688, 8691, 8692, 8693, 8694, 8695, 8696, 8697, 8698, 8699, 8701, 8715, 8716, 8717, 8719, 8720, 8722, 8723, 8725, 8739, 8755, 8756, 8757, 8758, 8759, 8760, 8761, 8784, 8787.
Products Sold
Serial Numbers: 8573, 8574, 8575, 8577, 8578, 8580, 8581, 8582, 8583, 8584, 8585, 8586, 8587, 8588, 8589, 8599, 8600, 8602, 8603, 8604, 8605, 8606, 8609, 8610, 8611, 8613, 8616, 8620, 8621, 8622, 8624, 8628, 8629, 8630, 8631, 8632, 8633, 8634, 8635, 8636, 8638, 8639, 8640, 8642, 8643, 8644, 8645, 8646, 8666, 8670, 8671, 8672, 8673, 8674, 8675, 8678, 8679, 8680, 8682, 8684, 8685, 8687, 8688, 8691, 8692, 8693, 8694, 8695, 8696, 8697, 8698, 8699, 8701, 8715, 8716, 8717, 8719, 8720, 8722, 8723, 8725, 8739, 8755, 8756, 8757, 8758, 8759, 8760, 8761, 8784, 8787.
Ossur H F Grjothals 5 Reykjavik Iceland is recalling Total Knee Junior Model Number 1100 Product Usage: The Total Knee Junior is an external polycentric due to Some units of the Total Knee Junior produced between November 25th, 2008 and through April, 2009 contain balancing units that may fail under extreme u. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Some units of the Total Knee Junior produced between November 25th, 2008 and through April, 2009 contain balancing units that may fail under extreme use over a long period. The fault is noncritical and no incidents or injuries resulting from this situation have been reported to Ossur at this stage. Over long term use (estimated to be in the four to six year range) the prosthetic device may fail a
Recommended Action
Per FDA guidance
Ossur sent a Safety Notice dated August 10, 2009 by mailed to all affected consignees. Ossur informed consignees of the above mentioned public reason for recall and asked consignees to take the following action: Identify the users of each of the Total Knee Junior model devices listed above and check inventory and isolate any recalled devices on hand but have not fitted on users. The letter states that Sue Fitzgerald from customer service will be contacting consignees in the next few days to coordinate replacement of the affected devices. For question call 1-(800) 219-2150, Ext: 4109. In addition, Ossur website: www.ossur.com we will be posting updates as appropriate.
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