Drugs & medicalClass II

United Orthopedic Corp. recalls Brand Name: U2 Total Knee System Product Name: Femoral valgus adaptor, left and right Model/Catalog Number: 9323-5333 and 9323-5334…

Due to an incomplete process of the component screw by a subcontractor which prevents the properly assembling of stem trail.

Read the official notice →
Date
2026-08-12
Country
United States
Brand
United Orthopedic
Product
Brand Name: U2 Total Knee System Product Name: Femoral valgus adaptor, left and right Model/Catalog Number: 9323-5333 and 9323-5334…
Classification
Class II
Units
US Nationwide distribution in the states of Texas and Michigan.
Category
Drugs & medical
Source
FDA · Device

Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer

What to do

  1. Check the product name, strength and lot number against the official notice.
  2. Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
  3. Ask the pharmacy or supplier about a replacement or refund.

General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.

More United Orthopedic recalls

  1. 2026-08-12
  2. US
    Drugs & medicalClass II

    United Orthopedic Corp. recalls Brand Name: U2 Total Knee System Product Name: Femoral offset bushing, 0mm and 4mm Model/Catalog Number: 9323-5310 Software Version: N/A…

    Due to a design issue causing the incorrect engraved numbering on implant that could result in the incorrect orientation of the implant.

    FDA · DeviceUnited Orthopedic Corp.US Nationwide distribution in the states of Texas and Michigan.Official notice →
  3. 2024-03-06
  4. US
    Drugs & medicalClass II

    United Orthopedic Corporation recalls USTAR II Knee System : Cemented Curved Stem, RHS Ti Plasma Spray, Reference Numbers: REF: PE25153109 - PE25151109 - 9x125mm,…

    Their is a potential that the implant curved stem may be oriented incorrectly.

    FDA · DeviceUnited Orthopedic CorporationUS: CA,KY, MI, IN, TN, CO, FL, TX, NV, OUS: Switzerland, United Kingdom,…Official notice →
All 3 United Orthopedic recalls →

Other drugs & medical recalls in the United States

  1. 2026-08-12
  2. US
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    Siemens Healthcare Diagnostics, Inc. recalls Atellica CH Urine Albumin REF: 11537225, in vitro diagnostic

    Processing of urine albumin assay on the CI analyzers may lead to the following issues: Falsely depressed Atellica CH Urea Nitrogen (UN_c) results; Falsely depressed Atellica CH Enzymatic Hemoglobin A1c (A1c_E)…

    FDA · DeviceSiemens Healthcare Diagnostics, Inc.Worldwide distribution - US Nationwide including Puerto Rico and the countries…Official notice →
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    Analyzers contain incorrect algorithms which may affect antimicrobial susceptibility test results, leading to false susceptibility classifications."

    FDA · DeviceBeckman Coulter Inc.US Nationwide distribution including in the states of AK, AL, AR, CA, CO, DE,…Official notice →
  4. US
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    FDA · DeviceHardy DiagnosticsU.S. Nationwide distribution in the states of AZ, CA, FL, ID, IN, MA, MS, NJ,…Official notice →
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    This recall is retroactively being reported. Refurbished bassinets failed to meet quality standards prior to distribution.

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    Drugs & medicalClass III

    Siemens Healthcare Diagnostics, Inc. recalls Syva Emit tox Serum Tricyclic Antidepressant Calibrator/Controls SMN 10445390 Catalog No. 7C219UL

    out-of-specification sodium azide concentration in Syva Emit Tox Serum Tricyclic Antidepressant Calibrator/Controls Lot U2. While the assay results were not impacted, the overall health risk to lab technicians due to…

    FDA · DeviceSiemens Healthcare Diagnostics, Inc.Worldwide - US Nationwide distribution in the states CA, ID, IL, IN, MA, MS,…Official notice →
  7. US
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    Siemens Healthcare Diagnostics, Inc. recalls Syva Emit Disopyramide Assay Enzyme Immunoassay, Lidocaine SMN 10445370 Catalog No 6N319UL

    Out-of-specification sodium azide concentration in Syva Emit Disopyramide Enzyme Immunoassay Calibrator Lot U1. While the assay results were not impacted, the overall health risk to lab technicians due to this issue is…

    FDA · DeviceSiemens Healthcare Diagnostics, Inc.Worldwide - US Nationwide distribution in the states of CA and VA. The country…Official notice →
See all drugs & medical recalls →