United Orthopedic Corporation recalls

6 recalls on record · latest: January 3, 2024

Official U.S. recall history for United Orthopedic Corporation, compiled from official government records.

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United Orthopedic Corporation recalls USTAR II Knee System : Cemented Curved Stem, RHS Ti Plasma Spray, Reference Numbers: REF: PE25153109 - PE25151109 - 9x1…

January 3, 2024 · Medical device recalls Moderate risk Their is a potential that the implant curved stem may be oriented incorrectly.

United Orthopedic Corporation recalls USTAR II Hip System Press-Fit Curved Stem, RHS Ti Plasma Spray for the following reference numbers: REF: PE11151211 - 1…

January 3, 2024 · Medical device recalls Moderate risk Their is a potential that the implant curved stem may be oriented incorrectly.

United Orthopedic Corporation recalls USTAR II Knee System Cemented curved stem, RHS, Non Coated for the following reference numbers: REF: PE25153109 - 9x125…

January 3, 2024 · Medical device recalls Moderate risk Their is a potential that the implant curved stem may be oriented incorrectly.

United Orthopedic Corporation recalls U2 Total Knee System Tibial Insert, Posterior Stabilized, #3, 11mm Thick Catalogue number 2303-3032 The U2 Total Knee s…

November 24, 2017 · Medical device recalls Moderate risk UOC received a customer compliant report from our distributor on October 31, 20…

United Orthopedic Corporation recalls U2 Total Knee System Tibial Insert, PSA, #1, 21mm Thick Catalogue number 2303-5016 The U2 Total Knee system is indicate…

November 24, 2017 · Medical device recalls Moderate risk UOC received a customer compliant report from our distributor on October 31, 20…

United Orthopedic Corporation recalls UOC Femoral Driver, Product number PE 93045101, orthopedic manual surgical instrument/accessory for use during surgery…

February 10, 2017 · Medical device recalls Moderate risk The locking lever pin component of the femoral driver may become deformed and b…