Class I — Serious Health Hazard

Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.

PROFEMUR PLUS CoCr MODULAR NECK Recalled by MicroPort Orthopedics, Inc. Due to Unexpected rate of postoperative fractures resulting in the...

Date: August 4, 2015
Company: MicroPort Orthopedics, Inc.
Status: Terminated
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 MicroPort Orthopedics, Inc. directly.

Affected Products

PROFEMUR PLUS CoCr MODULAR NECK, REF: PHAC1254, SIZE LONG, ORIENTATION 8 degree VAR/VAL. 12/14 SLT Taper. Orthopedic hip prosthesis component.

Quantity: 10,489 units

Why Was This Recalled?

Unexpected rate of postoperative fractures resulting in the need for revision surgery.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About MicroPort Orthopedics, Inc.

MicroPort Orthopedics, Inc. has 1 total recall tracked by RecallDetector.

Related Recalls

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