Zimmer Biomet, Inc.: Medical Device Recall in 2020 - (Recall #: Z-0871-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

ASI 2.0 Calcar Trimmer Shaft for Use with Zimmer Rasp Mode Number: 110032332 Product Usage: The device is a general orthopedic manual surgical instrument

Product Classification:

Class II

Date Initiated: December 19, 2019

Date Posted: February 5, 2020

Recall Number: Z-0871-2020

Event ID: 84598

Reason for Recall:

Potential issue associated with the instrument -end of the shaft could fail to effectively mate with the broach

Status: Terminated

Product Quantity: 67 units

Code Information:

Lot Numbers: 827310, 711160, 203240

Distribution Pattern:

US Nationwide and Foreign: countries of Canada, CHINA, NETHERLANDS

Voluntary or Mandated:

Voluntary: Firm initiated