Class II — Potential Health Hazard

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

5.5MM Arthrogarde Hip Access Cannula Recalled by Smith & Nephew, Inc. Due to The J Lock feature on the cannula body...

Date: September 21, 2020
Company: Smith & Nephew, 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 Smith & Nephew, Inc. directly.

Affected Products

5.5MM Arthrogarde Hip Access Cannula

Quantity: 143 units

Why Was This Recalled?

The J Lock feature on the cannula body was manufactured incorrectly, preventing the cannula from locking into an irrigation extender or arthroscope in the correct orientation.

Where Was This Sold?

This product was distributed to 20 states: CA, CO, CT, DE, GA, IL, IN, IA, MD, MO, NY, NC, OH, PA, SC, TN, TX, WA, WV, WI

Affected (20 states)Not affected

About Smith & Nephew, Inc.

Smith & Nephew, Inc. has 220 total recalls tracked by RecallDetector.

Related Recalls

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