Medartis, Inc.: Medical Device Recall in 2014 - (Recall #: Z-0150-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

Product Description:

APTUS Ulna Shortening 2.5 Product Usage: APTUS Ulna Shortening 2.5 Plates are indicated for fractures and osteotomies, in particular for the ulna.

Product Classification:

Class II

Date Initiated: October 1, 2014

Date Posted: November 5, 2014

Recall Number: Z-0150-2015

Event ID: 69433

Reason for Recall:

A recall of the APTUS Ulna Shortening 2.5 instrument was initiated due to three (3) complaints of breakage of the temporary tension bolt.

Status: Terminated

Product Quantity: 44

Code Information:

Part no. A-2791.05, lot no. 14125026

Distribution Pattern:

US Nationwide Distribution in the states of WV, IL, CT, AZ, and WA.

Voluntary or Mandated:

Voluntary: Firm initiated