Class II — Potential Health Hazard

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

4.0 mm Cancellous Screw Recalled by Zimmer, Inc. Due to Zimmer is recalling various trauma screws that failed...

Date: July 22, 2014
Company: Zimmer, 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 Zimmer, Inc. directly.

Affected Products

4.0 mm Cancellous Screw, Partially Threaded Sterile Zimmer

Quantity: 47,682 units total

Why Was This Recalled?

Zimmer is recalling various trauma screws that failed a leak test due to damage of the inner cavity only.

Where Was This Sold?

This product was distributed to 43 states: AL, AK, AZ, CA, CT, FL, GA, HI, ID, IL, IN, IA, KS, KY, LA, ME, MD, MA, MI, MN, MS, MO, MT, NE, NV, NJ, NM, NY, NC, OH, OK, OR, PA, SC, SD, TN, TX, VA, WA, WV, WI, WY, DC

Affected (43 states)Not affected

About Zimmer, Inc.

Zimmer, Inc. has 437 total recalls tracked by RecallDetector.

Related Recalls

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