Class II — Potential Health Hazard

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

Stryker SWANSON Flexspan Finger Joint Implant W/O Grommets Silicone Recalled by Wright Medical Technology, Inc. Due to An incorrect sizing label was applied to the...

Date: July 27, 2022
Company: Wright Medical Technology, Inc.
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 Wright Medical Technology, Inc. directly.

Affected Products

Stryker SWANSON Flexspan Finger Joint Implant W/O Grommets Silicone, Size: 00, REF 4700020, Sterile.

Quantity: 17 devices

Why Was This Recalled?

An incorrect sizing label was applied to the carton packaging.

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