Class II — Potential Health Hazard

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

Drill Recalled by Zimmer GmbH Due to An investigation identified that the products were possibly...

Date: April 8, 2019
Company: Zimmer GmbH
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 GmbH directly.

Affected Products

Drill, cannulated, 2.8x120mm, AO, Item Number ST502015628

Quantity: N/A

Why Was This Recalled?

An investigation identified that the products were possibly manufactured from a different material than defined in the applicable specifications.

Where Was This Sold?

This product was distributed to 42 states: AL, AZ, AR, CA, CO, FL, GA, HI, IL, IN, IA, KS, KY, LA, ME, MD, MA, MI, MN, MO, MT, NE, NV, NH, NJ, NM, NY, NC, ND, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WV, WI, WY

Affected (42 states)Not affected

About Zimmer GmbH

Zimmer GmbH has 85 total recalls tracked by RecallDetector.

Related Recalls

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