Zimmer Biomet, Inc.: Medical Device Recall in 2019 - (Recall #: Z-0517-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

ASI 2.0 Calcar Trimmer Shaft for Use with Biomet¿ Rasp, Model Number 110032331

Product Classification:

Class II

Date Initiated: August 6, 2019

Date Posted: December 4, 2019

Recall Number: Z-0517-2020

Event ID: 84124

Reason for Recall:

The potential that the end of the shaft could fail to effectively mate with the broach with the Calcar Planar Shaft instrument, part number 110032331.

Status: Terminated

Product Quantity: 73

Code Information:

Model Number: 11032331 Lots: 784060, 662870

Distribution Pattern:

CA, IN, MN, NJ, NY, AR, LA, OH, KY, TX, CO (US) CA, CN, NL (International)

Voluntary or Mandated:

Voluntary: Firm initiated