Aesculap, Inc.: Medical Device Recall in 2013 - (Recall #: Z-0361-2014)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2013.

Data Source: FDA.

Product Description:

Aesculap Arcadius XP L Trial Insertion Instrument (ME020R/ME020R-US)

Product Classification:

Class II

Date Initiated: September 20, 2013

Date Posted: November 27, 2013

Recall Number: Z-0361-2014

Event ID: 66534

Reason for Recall:

The trial insertion instrument may disassemble during use due to a potentially weak weld on then trial inserter shaft block area located near the thumb wheel.

Status: Terminated

Product Quantity: 30

Code Information:

model no. ME020R

Distribution Pattern:

Worldwide distribution: USA (nationwide) GA, TN, CA, WY, NV, TX, OK, OH, and IL; and internationally to Canada.

Voluntary or Mandated:

Voluntary: Firm initiated