Zimmer CAS: Medical Device Recall in 2015 - (Recall #: Z-1701-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

Product Description:

Tibial Alignment Guide; Orthopedic Stereotaxic Instrument;

Product Classification:

Class II

Date Initiated: April 19, 2015

Date Posted: June 10, 2015

Recall Number: Z-1701-2015

Event ID: 71202

Reason for Recall:

Zimmer CAS has determined that the potential exists for the spikes on the iASSIST Tibial Alignment Guide to bend or break during insertion or extraction from the tibia during use.

Status: Terminated

Product Quantity: 78 devices

Code Information:

Item Number: 20-8011-013-00; Lot Numbers: 120265; 110623; 120659; 120794;120659-1; 130134; 120793; 130135

Distribution Pattern:

Nationwide Distribution including AL, AZ, CA, CA, CO, FL, IN, MI, NJ, NY, OH, OR, PA, TX, VA, and WI.

Voluntary or Mandated:

Voluntary: Firm initiated