UNITED ORTHOPEDIC CORPORATION
5 recall(s) on record — most severe on record: Class II.
Recalls by year
- Recalls (5)
Registered facilities (3)
- UNITED ORTHOPEDIC CORPORATION FEI 3012329926 · TW
- UOC USA Inc. FEI 3009760038 · CA
- UNITED ORTHOPEDIC CORP. FEI 1000395711 · TW
Recalls & enforcement
- Class IIOngoing2026-05-20Due to an incomplete process of the component screw by a subcontractor which prevents the properly assembling of stem trail.
- Class IIOngoing2026-03-19Due to a design issue causing the incorrect engraved numbering on implant that could result in the incorrect orientation of the implant.
- Class IIOngoing2024-01-03Their is a potential that the implant curved stem may be oriented incorrectly.
- Class IITerminated2017-11-24UOC 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.
- Class IITerminated2017-02-10The 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.
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. We restate the public record only — measured facts, never risk verdicts.
Cite this record
RegWarden. “UNITED ORTHOPEDIC CORPORATION — FDA compliance profile.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/company/oo-9025838-united-orthopedic-corporation/
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