# FDA recall Z-2662-2017

> **Exactech, Inc.** · Class II · device recall initiated 2017-05-25.

## Product

Logic Fit Tibial Tamp Head

## Reason for recall

The firm determined that the labeling (surgical technique) should be updated to clarify the proper technique and instrumentation to remove the tamp assembly from the bone, i.e., to include a caution statement about the potential for instrument breakage if the tamp handle/guide is misused by impacting in retro-grade.

## Distribution

AL, AZ, CA, CA, CO, FL, GA, IA, ID, IL, IN, KS, LA, MA, MD, ME, MN, NC, NJ, NV, NY, OH, OK, OR, RI, SC, TN, TX, VA, WA, WI, Hawaii and Puerto Rico  Australia, France, Germany, India, Italy, Japan, Korea, Luxembourg, Singapore,  Spain, Switzerland, The Netherlands and United Kingdom

## Key facts

- **Recall number:** Z-2662-2017
- **Recalling firm:** Exactech, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-05-25
- **Report date:** 2017-07-12
- **Termination date:** 2019-07-26

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2662-2017

## Citation

> AI Analytics. FDA recall Z-2662-2017. Retrieved 2026-07-17 from https://api.ai-analytics.org/recall/Z-2662-2017. Source: US FDA. Licensed CC0.

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