Biomet: Medical Device Recall in 2020 - (Recall #: Z-2303-2020)

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:

Biomet 6.5 Cannulated Screw Tap - Bone fixation screw, Item Number: 110008466 - Product Usage: Intended for temporary internal fixation and stabilization of osteotomies and fractures during the normal healing process.

Product Classification:

Class II

Date Initiated: May 14, 2020

Date Posted: June 17, 2020

Recall Number: Z-2303-2020

Event ID: 85701

Reason for Recall:

Distributed to the field without having completed design history files or design transfer activities

Status: Terminated

Product Quantity: 6 OUS

Code Information:

Lot Number: 624820 (01)00887868133732(17)260415(10)624820 867200 (01)00887868133732(17)260731(10)867200

Distribution Pattern:

Worldwide distribution - US Nationwide distribution including in the states of NY, GA, FL, MO and the countries of Canada, AUSTRALIA, CHILE, CHINA, JAPAN, MALAYSIA, NETHERLANDS.

Voluntary or Mandated:

Voluntary: Firm initiated