Zimmer Biomet, Inc.: Medical Device Recall in 2018 - (Recall #: Z-2365-2018)

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:

Zimmer¿ M/L Taper Hip Prosthesis With Kinective¿ Technology Cementless, Size 10; 00-7713-010-00

Product Classification:

Class II

Date Initiated: May 30, 2018

Date Posted: July 11, 2018

Recall Number: Z-2365-2018

Event ID: 80188

Reason for Recall:

Status: Terminated

Product Quantity: 24

Code Information:

62361460 62528141

Distribution Pattern:

Products were distributed solely to Japan.

Voluntary or Mandated:

Voluntary: Firm initiated