Zimmer Biomet, Inc.: Medical Device Recall in 2018 - (Recall #: Z-1306-2018)

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:

A.L.P.S. MIS Calcaneus Locking Plate LG RT F.A.S.T. Guide inserts, Item Number: 816209003,UDI: 00887868044670989403

Product Classification:

Class II

Date Initiated: October 25, 2017

Date Posted: April 11, 2018

Recall Number: Z-1306-2018

Event ID: 79393

Reason for Recall:

The drill guides were manufactured with the incorrect color anodization.

Status: Terminated

Product Quantity: 22

Code Information:

Package Lot: 989430; Lot Etched on Product: P0284

Distribution Pattern:

Distributed in the following US States: AZ, MO, MT, NJ, NY, OH, TX, and WA. Distributed in Chile and Netherlands.

Voluntary or Mandated:

Voluntary: Firm initiated