The Anspach Effort, Inc.: Medical Device Recall in 2012 - (Recall #: Z-0075-2013)

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 with Direction Only***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-0075-2013

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: 41 units

Code Information:

Serial Numbers: E28305271001, E28305271002, E28305271003, E28305271004, E2830527100, E28305271006, E28305271007, E28305271008, E2830521009, E28305271010, E29305270901, E29305270902, E29305270903, E29305271101, E29305271102, E29305271103, E29305271104, E29305271105, E29305271106, E29305271107, E29,

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated