# FDA recall Z-2741-2017

> **Mako Surgical Corporation** · Class II · device recall initiated 2017-06-07.

## Product

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

## Reason for recall

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

## Distribution

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

## Key facts

- **Recall number:** Z-2741-2017
- **Recalling firm:** Mako Surgical Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-06-07
- **Report date:** 2017-07-26
- **Termination date:** 2020-06-16

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Davie, FL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2741-2017

## Citation

> AI Analytics. FDA recall Z-2741-2017. Retrieved 2026-06-08 from https://api.ai-analytics.org/recall/Z-2741-2017. Source: US FDA. Licensed CC0.

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