# FDA recall Z-2745-2020

> **Mako Surgical Corporation** · Class II · device recall initiated 2020-07-09.

## Product

Mako Hip End Effector, Variable Angle  Catalog Number: 206967  GTIN:00848486022167

## Reason for recall

Characterization issue associated with the product.  This issue may cause a discrepancy during bone preparation in certain Mako Total Hip procedures.

## Distribution

TX, MN, CA, RI, FL, NY, AZ, TN

## Key facts

- **Recall number:** Z-2745-2020
- **Recalling firm:** Mako Surgical Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-07-09
- **Report date:** 2020-08-12
- **Termination date:** 2023-06-16

- **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-2745-2020

## Citation

> AI Analytics. FDA recall Z-2745-2020. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-2745-2020. Source: US FDA. Licensed CC0.

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