Zimmer Biomet, Inc.: Medical Device Recall in 2018 - (Recall #: Z-2875-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

Connecting Bolt, Model 14-442093

Product Classification:

Class II

Date Initiated: June 18, 2018

Date Posted: August 29, 2018

Recall Number: Z-2875-2018

Event ID: 80543

Reason for Recall:

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.

Status: Terminated

Product Quantity: 247 units

Code Information:

...

Distribution Pattern:

AR, AZ, CA, FL, GA, IN, KY, LA, MA, MI, MN, MO, MT, NJ, NY, OH, SC, TX, UT & WI

Voluntary or Mandated:

Voluntary: Firm initiated