Class II — Potential Health Hazard

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

PHALINX (TM) HAMMERTOE HANDLE Recalled by Wright Medical Technology, Inc. Due to The term DORSAL was laser etched on the...

Date: April 16, 2015
Company: Wright Medical Technology, 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 Wright Medical Technology, Inc. directly.

Affected Products

PHALINX (TM) HAMMERTOE HANDLE, SIZE: SMALL, STYLE: ANGLED, REF 45304012, CONTENTS 1 EACH, RX ONLY

Quantity: 121 units

Why Was This Recalled?

The term DORSAL was laser etched on the incorrect side on some of the angled handles.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Wright Medical Technology, Inc.

Wright Medical Technology, Inc. has 69 total recalls tracked by RecallDetector.

Related Recalls

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