# FDA recall Z-1824-2019

> **Mako Surgical Corporation** · Class II · device recall initiated 2019-04-25.

## Product

2.7 Degree Straight Sagittal Saw attachment (Mako Total Knee Application and Partial Knee Application 3.0)

## Reason for recall

The bearings of the saw attachments were ungreased.

## Distribution

AR, CA, FL, KS, MA, MO, NC, NJ, NY, OH, OR, TN, and TX.  Australia, China and Netherlands

## Key facts

- **Recall number:** Z-1824-2019
- **Recalling firm:** Mako Surgical Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-04-25
- **Report date:** 2019-06-26
- **Termination date:** 2021-04-22

- **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-1824-2019

## Citation

> AI Analytics. FDA recall Z-1824-2019. Retrieved 2026-06-03 from https://api.ai-analytics.org/recall/Z-1824-2019. Source: US FDA. Licensed CC0.

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