Medical device recalls Moderate risk

Zimmer Biomet, Inc. recalls Connecting Bolt, Model 14-442093

Recall date
June 18, 2018
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-2875-2018
FDA classification
Class II
Brand / firm
Zimmer Biomet, Inc.
Sold / distributed
AR, AZ, CA, FL, GA, IN, KY, LA, MA, MI, MN, MO, MT, NJ, NY, OH, SC, TX, UT & WI

Why it was recalled

Product was manufactured from the incorrect material, which shows a potential decrease in the fatigue strength of the connecting bolt that can lead to fracture.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Connecting Bolt, Model 14-442093

Get recall alerts

Free email alert whenever Zimmer Biomet, Inc. has a new recall — straight from official government data. Unsubscribe anytime.

More recalls from: Zimmer Biomet, Inc.