Orthosoft, Inc. dba Zimmer CAS: Medical Device Recall in 2017 - (Recall #: Z-1868-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

SmartTools Knee System Orthopedic Stereotaxic Instrument

Product Classification:

Class II

Date Initiated: February 20, 2017

Date Posted: April 26, 2017

Recall Number: Z-1868-2017

Event ID: 76508

Reason for Recall:

There has been an increase in the number of complaints regarding bent or broken Drive Pins of the Validation Tool manufactured with drawing Revision M to P

Status: Terminated

Product Quantity: 84

Code Information:

Lots: 130542A1 1405941 140146 140146-1 140147 140407A 140407A-1 140407B 140407-B-1 140860 140860-1 141035 150120 B150120 B150711

Distribution Pattern:

Nationwide Distribution

Voluntary or Mandated:

Voluntary: Firm initiated