The Anspach Effort, Inc.: Medical Device Recall in 2012 - (Recall #: Z-0074-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2012.

Data Source: FDA.

Product Description:

"***Electric Systems Foot Control****Rx Only***" Product Usage: Cutting and shaping bone including bones of the spine and cranium.

Product Classification:

Class II

Date Initiated: January 9, 2012

Date Posted: October 24, 2012

Recall Number: Z-0074-2013

Event ID: 63086

Reason for Recall:

The Anspach Effort, Inc. in Palm Beach Gardens, FL is recalling the foot control/foot pedal due to the Foot Control Cable lacking the shield connection from the cable to the connector body.

Status: Terminated

Product Quantity: 16 units

Code Information:

Serial Numbers: E31305311301, E31305311302, E31305311303, E31305311304, E31305311401, E31305311402, E31305311403, E31305311404, E31305311405, E32305311201, E32305311202, E33305311501, E33305311502, E33305311504, and E33305311505

Distribution Pattern:

Worldwide Distribution - US (nationwide) and the countries of: Italy, Japan, Switzerland, Turkey and Taiwan.

Voluntary or Mandated:

Voluntary: Firm initiated