United Orthopedic Corporation
Complete recall history across all FDA and CPSC categories — 6 total recalls
United Orthopedic Corporation appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.
Device Recalls (6)
FDA medical device enforcement actions by United Orthopedic Corporation
| Date | Product | Reason | Class |
|---|---|---|---|
| Jan 3, 2024 | USTAR II Knee System Cemented curved stem, RHS, Non Coated for the following ... | Their is a potential that the implant curved stem may be oriented incorrectly. | Class II |
| Jan 3, 2024 | USTAR II Hip System Press-Fit Curved Stem, RHS Ti Plasma Spray for the follow... | Their is a potential that the implant curved stem may be oriented incorrectly. | Class II |
| Jan 3, 2024 | USTAR II Knee System : Cemented Curved Stem, RHS Ti Plasma Spray, Reference N... | Their is a potential that the implant curved stem may be oriented incorrectly. | Class II |
| Nov 24, 2017 | U2 Total Knee System Tibial Insert, PSA, #1, 21mm Thick Catalogue number 2303... | UOC received a customer compliant report from our distributor on October 31, ... | Class II |
| Nov 24, 2017 | U2 Total Knee System Tibial Insert, Posterior Stabilized, #3, 11mm Thick Cat... | UOC received a customer compliant report from our distributor on October 31, ... | Class II |
| Feb 10, 2017 | UOC Femoral Driver, Product number PE 93045101, orthopedic manual surgical in... | The locking lever pin component of the femoral driver may become deformed and... | Class II |
Frequently Asked Questions
A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.
Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.
The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.
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