The Anspach Effort, Inc.: Medical Device Recall in 2016 - (Recall #: Z-0747-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

Synthes Small Electric Drive (SED). For use in general traumatology.

Product Classification:

Class II

Date Initiated: August 14, 2014

Date Posted: February 10, 2016

Recall Number: Z-0747-2016

Event ID: 73000

Reason for Recall:

The affected Small Electric Drive (SED) may operate solely in reverse mode, not operate in reverse mode when intended, not function, or unintentionally start.

Status: Terminated

Product Quantity: 599 each

Code Information:

All Lots

Distribution Pattern:

Worldwide Distribution-US (nationwide) including the states of AR, AZ, CA, CO, FL, ID, IL, KS, LA, MI, NC, NY, TX, WA, VA and HI, and the countries of Germany, Hong Kong, Chile, Israel, Poland, Italy, Turkey, Italy, Singapore, Ireland, Korea, Spain, Norway, Denmark, Great Britain, Finland, Belgium, Netherlands, France, Japan, Sweden, Switzerland, Austria, China, India, Thailand, Russia, New Zealand, Zaire, Australia, Taiwan, and Malaysia.

Voluntary or Mandated:

Voluntary: Firm initiated