Home / Brands / United Orthopedic
United Orthopedic Recalls
12 recalls on record · April 5, 2017 to August 12, 2026 · Medical Devices
Recalls by year
17
18
24
26
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
August 12, 2026Medical DevicesFDA
United Orthopedic Corp. recalls Brand Name: U2 Total Knee System Product Name: Femoral offset bushing, 2mm and 6mm Model/Catalog Number: 9323-5312 So
Hazard: Due to a design issue causing the incorrect engraved numbering on implant that could result in the incorrect orientation of the implant.
August 12, 2026Medical DevicesFDA
United Orthopedic Corp. recalls Brand Name: U2 Total Knee System Product Name: Femoral offset bushing, 0mm and 4mm Model/Catalog Number: 9323-5310 So
Hazard: Due to a design issue causing the incorrect engraved numbering on implant that could result in the incorrect orientation of the implant.
August 12, 2026Medical DevicesFDA
United Orthopedic Corp. recalls Brand Name: U2 Total Knee System Product Name: Femoral valgus offset adaptor, 2mm, 4mm, 6mm, left and Femoral valgus of
Hazard: Due to an incomplete process of the component screw by a subcontractor which prevents the properly assembling of stem trail.
August 12, 2026Medical DevicesFDA
United Orthopedic Corp. recalls Brand Name: U2 Total Knee System Product Name: Femoral valgus adaptor, left and right Model/Catalog Number: 9323-5333
Hazard: Due to an incomplete process of the component screw by a subcontractor which prevents the properly assembling of stem trail.
August 12, 2026Medical DevicesFDA
United Orthopedic Corp. recalls Brand Name: USTAR II Knee System Product Name: Hinge Box Trial, L, #1-6 and Hinge Box Trial, R, #1-6 Model/Catalog Num
Hazard: Due to an incomplete process of the component screw by a subcontractor which prevents the properly assembling of stem trail.
August 12, 2026Medical DevicesFDA
United Orthopedic Corp. recalls Brand Name: U2 Total Knee System Product Name: PSA Box Trial, L, #1-6 and PSA Box Trial, R, #1-6 Model/Catalog Number:
Hazard: Due to an incomplete process of the component screw by a subcontractor which prevents the properly assembling of stem trail.
March 6, 2024Medical DevicesFDA
United Orthopedic Corporation recalls USTAR II Knee System : Cemented Curved Stem, RHS Ti Plasma Spray, Reference Numbers: REF: PE25153109 - PE25151109 -
Hazard: Their is a potential that the implant curved stem may be oriented incorrectly.
March 6, 2024Medical DevicesFDA
United Orthopedic Corporation recalls USTAR II Knee System Cemented curved stem, RHS, Non Coated for the following reference numbers: REF: PE25153109 - 9x1
Hazard: Their is a potential that the implant curved stem may be oriented incorrectly.
March 6, 2024Medical DevicesFDA
United Orthopedic Corporation recalls USTAR II Hip System Press-Fit Curved Stem, RHS Ti Plasma Spray for the following reference numbers: REF: PE11151211 -
Hazard: Their is a potential that the implant curved stem may be oriented incorrectly.
March 28, 2018Medical DevicesFDA
United Orthopedic Corporation recalls U2 Total Knee System Tibial Insert, PSA, #1, 21mm Thick Catalogue number 2303-5016 The U2 Total Knee system is indica
Hazard: UOC received a customer compliant report from our distributor on October 31, 2017 which stated that contents of the package do not match the product labeling.
March 28, 2018Medical DevicesFDA
United Orthopedic Corporation recalls U2 Total Knee System Tibial Insert, Posterior Stabilized, #3, 11mm Thick Catalogue number 2303-3032 The U2 Total Kne
Hazard: UOC received a customer compliant report from our distributor on October 31, 2017 which stated that contents of the package do not match the product labeling.
April 5, 2017Medical DevicesFDA
United Orthopedic Corporation recalls UOC Femoral Driver, Product number PE 93045101, orthopedic manual surgical instrument/accessory for use during surgery t
Hazard: The locking lever pin component of the femoral driver may become deformed and break, resulting in malfunction during surgery and causing the device to become inoperable.