Mako Surgical Corporation: Medical Device Recall in 2017 - (Recall #: Z-2741-2017)

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:

MAKO RIO Standard System, internal cPCI Card CageP/N: 201337. Intended to assist the surgeon in providing software defined spatial boundaries during orthopedic procedures.

Product Classification:

Class II

Date Initiated: June 7, 2017

Date Posted: July 26, 2017

Recall Number: Z-2741-2017

Event ID: 77553

Reason for Recall:

An intermittent electrical problem that could lead to a loss of system power due to a loose screw connection.

Status: Terminated

Product Quantity: 20

Code Information:

Lot No. 05212015

Distribution Pattern:

Distributed to the states of AZ, CA, CO, CT, FL, GA, ID, LA, MA, MO, MS, NC, OH, PA, TN, TX, & WA.

Voluntary or Mandated:

Voluntary: Firm initiated