The Recall Desk

Manufacturer

United Orthopedic Corporation

6 recalls in our database name United Orthopedic Corporation as the manufacturing or recalling firm.

What the numbers show

Total
6
Critical
0
Severe
0
Most recent
2024-03-06

Of the 6 recalls from United Orthopedic Corporation we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 0 (0%) are Severe.

About this listing

The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.

Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.

1–6 of 6

  • HighFDA (Devices)·Z-1216-2024·2024-03-06

    USTAR II Knee System implants recalled for potential stem misalignment

    The FDA is recalling USTAR II Knee System implants due to potential incorrect orientation of the curved stem. The defect may affect proper implant positioning in knee replacement surgery.

    Product
    USTAR II Knee System Cemented curved stem, RHS, Non Coated for the following reference numbers: REF: PE25153109 - 9x125mm, PE25153209 - 9x150mm, PE25153113 - 13x125mm, PE25153111- 11x125mm, PE25153115 - 15x125mm, PE25153211 - 11x150mm, PE25153213 - 13x150mm, PE25153217 - 17x1
    Category
    Medical Device
    Distribution
    9 states
  • HighFDA (Devices)·Z-1215-2024·2024-03-06

    Hip Implant System Recalled for Potential Incorrect Stem Orientation

    United Orthopedic Corporation is recalling the USTAR II Hip System Press-Fit Curved Stem due to a potential risk that the implant curved stem may be oriented incorrectly. The FDA Class II recall affects 598 units.

    Product
    USTAR II Hip System Press-Fit Curved Stem, RHS Ti Plasma Spray for the following reference numbers: REF: PE11151211 - 11x150mm, PE11151213 - 13x150mm, PE11151215 - 15x150mm, PE11151217 - 17x150mm, PE11151411 - 11x200mm, PE11151413 - 13x200mm, PE11151415 - 15x200mm, PE11151417
    Category
    Medical Device
    Distribution
    9 states
  • HighFDA (Devices)·Z-1217-2024·2024-03-06

    Orthopedic knee implant recall due to potential stem misalignment

    United Orthopedic Corporation recalls USTAR II knee implants due to potential incorrect orientation of the curved stem. Affected products were distributed across multiple US states and internationally.

    Product
    USTAR II Knee System : Cemented Curved Stem, RHS Ti Plasma Spray, Reference Numbers: REF: PE25153109 - PE25151109 - 9x125mm, PE25151111 - 11X125, PE25151113 - 13X125mm, PE25151115 - 15X125mm, PE25151117 - 17X125mm, PE25151119 - 19X125mm, PE25151209 - 9X150mm, PE25151211 - 11
    Category
    Medical Device
    Distribution
    9 states
  • ModerateFDA (Devices)·Z-1128-2018·2018-03-28

    United Orthopedic Recalls U2 Total Knee System Tibial Inserts Due to Labeling Mismatch

    United Orthopedic Corporation is recalling 69 U2 Total Knee System Tibial Inserts because the package contents did not match the product labeling.

    Product
    U2 Total Knee System Tibial Insert, Posterior Stabilized, #3, 11mm Thick Catalogue number 2303-3032 The U2 Total Knee system is indicated in knee arthroplasty for reduction or relief of pain and/or improved knee function in skeletally mature patients with severe knee pain and
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1129-2018·2018-03-28

    United Orthopedic Recalls U2 Total Knee System Tibial Inserts

    United Orthopedic Corporation is recalling 14 U2 Total Knee System Tibial Inserts because the package contents did not match the product labeling.

    Product
    U2 Total Knee System Tibial Insert, PSA, #1, 21mm Thick Catalogue number 2303-5016 The U2 Total Knee system is indicated in knee arthroplasty for reduction or relief of pain and/or improved knee function in skeletally mature patients with severe knee pain and disability due to
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1692-2017·2017-04-05

    UOC Femoral Driver Recalled Due to Locking Lever Pin Breakage Risk

    United Orthopedic Corporation is recalling 33 UOC Femoral Drivers because the locking lever pin may deform and break, causing the device to malfunction during surgery.

    Product
    UOC Femoral Driver, Product number PE 93045101, orthopedic manual surgical instrument/accessory for use during surgery to implant femoral components and femoral trial, and to remove femoral trial.
    Category
    Medical Device
    Distribution
    1 state

About this company

Community-sourced company facts from Wikidata, not from any recall agency. This is background on the corporate entity — it says nothing about the recall(s) listed on this page, which come from the agency source notice above.

United Orthopedic (Taiwan)

company in New Taipei, Taiwan

Country
Taiwan
Founded
1993

Official website

Source: Wikidata (Q137204476), licensed CC0. Wikidata is community-edited and may not reflect the current corporate structure.