Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

USTAR II Hip System Press-Fit Curved Stem Recalled by United Orthopedic Corporation Due to Their is a potential that the implant curved...

Date: January 3, 2024
Company: United Orthopedic Corporation
Status: Ongoing
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact United Orthopedic Corporation directly.

Affected Products

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 - 17x200mm,

Quantity: 598 units

Why Was This Recalled?

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

Where Was This Sold?

This product was distributed to 9 states: CA, CO, FL, IN, KY, MI, NV, TN, TX

Affected (9 states)Not affected

About United Orthopedic Corporation

United Orthopedic Corporation has 6 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report