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Medartis, Inc. recalls APTUS Ulna Shortening 2.5 Product Usage: APTUS Ulna Shortening 2.5 Plates are indicated for fractures and osteotomi
Recalled November 5, 2014 · FDA recall Z-0150-2015 · Medartis
Hazard
A recall of the APTUS Ulna Shortening 2.5 instrument was initiated due to three (3) complaints of breakage of the temporary tension bolt. · FDA Class II
Units
44
Sold at
US Nationwide Distribution in the states of WV, IL, CT, AZ, and WA.
Description
A recall of the APTUS Ulna Shortening 2.5 instrument was initiated due to three (3) complaints of breakage of the temporary tension bolt.
Product
APTUS Ulna Shortening 2.5 Product Usage: APTUS Ulna Shortening 2.5 Plates are indicated for fractures and osteotomies, in particular for the ulna.
Manufacturer(s)
Medartis, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →