Class II — Potential Health Hazard

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

MAKOplasty Hip Array Kit Laminate 150230 Recalled by Mako Surgical Corporation Due to Stryker Orthpaedics became aware that there is the...

Date: November 25, 2015
Company: Mako Surgical Corporation
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 Mako Surgical Corporation directly.

Affected Products

MAKOplasty Hip Array Kit Laminate 150230

Quantity: 10 units.

Why Was This Recalled?

Stryker Orthpaedics became aware that there is the potential for the 210540 MAKOplasty Hip Array Kit Laminate 150230 to list two part numbers for the RIO Base Array, which is item #5 on the product table.

Where Was This Sold?

This product was distributed to 5 states: CO, KY, MN, WA, WV

Affected (5 states)Not affected

About Mako Surgical Corporation

Mako Surgical Corporation has 27 total recalls tracked by RecallDetector.

Related Recalls

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