Due to packaging discrepancy with the incorrect tibial inserts/implants being packaged. The use of this product may result in the incorrect product being selected. This could result in a revision surgery if used.
Reason for recall: Due to packaging discrepancy with the incorrect tibial inserts/implants being packaged. The use of this product may result in the incorrect product being selected. This could result in a revision surgery if used. Distribution: U.S Distribution to states of: AZ, IA, ID, IL, IN, LA, MI, MO, MS, NE, NY, OK, OR, PR, SD, UT, VA, and WA Quantity: 20 Lot/code info: Lot Code: Item: 341-10-711 GTIN: 00888912166881 Lot\s: 071T1084
00888912166881
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.