FDAFDA recall Z-2885-2026 · Aug 12, 2026
United Orthopedic Corp.: Brand Name: U2 Total Knee System Product Name: Femoral valgus adaptor recall
Recall found
Product
Brand Name: U2 Total Knee System Product Name: Femoral valgus adaptor, left and right Model/Catalog Number: 9323-5333 and 9323-5334 Software Version: N/A Product Description: Manual Orthopedic Surgical Instrument Component: No
Reason for recall
Due to an incomplete process of the component screw by a subcontractor which prevents the properly assembling of stem trail.
What to do
FDA enforcement reports don't include consumer instructions. Check the codes below against your packaging. If this is a medicine or device you use, talk to your pharmacist or doctor before you stop or change anything, and contact the company or FDA for what to do with the product.
Recall details
- FDA classification
- Class II: use of or exposure to the product may cause temporary or medically reversible health problems, or the chance of serious problems is remote.
- Status
- Ongoing
- Codes, lots and dates
- Product Number; UDI-DI Code; Lot Code: Product number 9323-5333; UDI-DI 04719886908084; Lot number 25FB50 Product number 9323-5334; UDI-DI 04719886908091; Lot number 25FB51
- Quantity
- 2
- Distribution
- US Nationwide distribution in the states of Texas and Michigan.
- Recalling firm
- United Orthopedic Corp., Kaohsiung
- Voluntary or mandated
- Voluntary: Firm initiated
- Recall started
- 2026-05-20
Source: openFDA enforcement record Z-2885-2026 · search recall number Z-2885-2026 in FDA's Enforcement Report.
Copied from the agency record without changes. Data as of Oct 22, 2026, 4:56 AM EDT. The agency notice is the final word.