Biomet recalls Biomet 6.5 Cannulated Screw Tap - Bone fixation screw, Item Number: 110008466 - Product Usage: Intended for temporary i…

Recall date

May 14, 2020

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-2303-2020

FDA classification

Class II

Brand / firm

Biomet

Sold / distributed

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.

Why it was recalled

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

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

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.