The Anspach Effort, Inc.: Medical Device Recall in 2014 - (Recall #: Z-0779-2014)

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:

Anspach MIA 16 (16cm Minimally Invasive Attachment), Rx Only MIA16 attachments are intended for use with Motor Systems for cutting and shaping bones, including the spine and cranium.

Product Classification:

Class II

Date Initiated: May 6, 2013

Date Posted: January 22, 2014

Recall Number: Z-0779-2014

Event ID: 67179

Reason for Recall:

Product did not reach expected sterility assurance level

Status: Terminated

Product Quantity: 183

Code Information:

ALL LOTS

Distribution Pattern:

Nationwide Distribution: FL, IL, CA. IN, MI, CA, NJ, TX, NE, NC, OR, PA, TN, DC, UT, CO, MO, KY, MD, WV, NY, and MN.

Voluntary or Mandated:

Voluntary: Firm initiated