Class II — Potential Health Hazard

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

Nonabsorbable suture anchor system intended to reattach soft tissue to Recalled by ConMed Corporation Due to Manufactured with the incorrect anchor outer body

Date: April 17, 2017
Company: ConMed 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 ConMed Corporation directly.

Affected Products

Nonabsorbable suture anchor system intended to reattach soft tissue to bone in orthopedic surgical procedures may be used in either arthroscopic or open surgical procedures.

Quantity: 56 units

Why Was This Recalled?

Manufactured with the incorrect anchor outer body

Where Was This Sold?

This product was distributed to 10 states: CA, IN, KS, MD, NY, OH, PA, TN, TX, WI

Affected (10 states)Not affected

About ConMed Corporation

ConMed Corporation has 69 total recalls tracked by RecallDetector.

Related Recalls

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