Oxford knee replacement recall

A recalled knee replacement system has kicked off new product liability.

For Additional Information Contact. Manufacturer Parent Company (2017) Zimmer Biomet Holdings. Recall Status 1: Terminated 3 on June 30, 2018: Recall Number: Z-1174. Manufacturer Reason. The Oxford PKR has more than 300 publications and the Oxford Cementless Partial Knee has demonstrated 10. Knee-replacement surgery is an increasingly common procedure: more than 650 000 total knee replacements (TKRs) were done in the USA in 2008, 1 more than 77 500 in the UK in 2009, 2 and 103 601 in South Korea between 2002 and 2005. Knee replacement Find out what a knee replacement involves, when it might be recommended, and how it can help with knee pain and movement. .

. class=" fc-falcon">Introduction. . DOI: 10. Manufacturer Reason. Escapule. Food and Drug Administration (FDA) is reminding patients and health care providers about Exactech joint replacement devices manufactured by Exactech between.

Product Description.

LINK SLED Knee System: ALL POLY TIBIAL COMPONENT 13MM X 55MM Item Number: 15-2028/12. GBLT07107 Rev 1 Ref: GBLW07101 Global Field Action Activities Page 1 of 9 ZFA 2022-00240. Manufacturer comment.

.

Recall of Device Recall Oxford Fixed Bearing Partial Knee Replacement According to.