ClearanceBrief
Recall Z-2147-2020 ยท JDI Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented

Biomet, Inc.

Knee Products: 150414 Orthopedic Salvage System (OSS) Tibial Bearing, 20 MM Standard - Product Usage: Knee prosthesis

DateApr 17, 2020
StatusTerminated
ReasonPotential presence of elevated endotoxin levels that exceed the specification limit
Root causeProcess control
ActionZimmer Biomet issued Urgent Medical Device recall letter dated April 17, 2002 to distributors with direct sales and/or field inventory via email and traceable letter sent via FedEx. Hospitals with direct sales or current inventory, as well as hospitals that have consumed products will be notified via FedEx. Surgeons that have consumed products will be notified via FedEx. Action to take: 1. Review this notification and ensure that affected team members are aware of the contents. 2. Immediately locate and quarantine affected product in your inventory. 3. Immediately return all affected product
Quantity12 units
DistributionWorldwide distribution - US Nationwide distribution and the countries of Canada, AHMADABAD, GUJARAT, BANGKOK, BELROSE NSW, BUENOS AIRES, CHILE, COSTA RICA, HIRATSUKA CITY, HUECHURABA SANTIAGO, INDIA, JAPAN, MEXICO DF, NETHERLANDS, PICHINCHA, EC, SAN JOSE,
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K002757ONCOLOGY SALVAGE SYSTEM
Biomet, Inc., Nov 24, 2000