# FDA recall Z-1676-2020

> **Synvasive Technology Inc** · Class II · device recall initiated 2018-07-27.

## Product

ZIMMER Oscillating Saw Blade -Cutting 75mm x 19mm x 1.00/1.27mm.intended for bone or cartilage in orthopedic procedures.   Manufactured By:  Synvasive Technology, Inc., a Subsidiary of Zimmer

## Reason for recall

Mislabeled: Actual blade width is 19 mm but the label indicates a width of 25 mm.

## Distribution

US distribution to states of AL and NY

## Key facts

- **Recall number:** Z-1676-2020
- **Recalling firm:** Synvasive Technology Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-07-27
- **Report date:** 2020-04-15
- **Termination date:** 2021-06-07

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** El Dorado Hills, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1676-2020

## Citation

> AI Analytics. FDA recall Z-1676-2020. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-1676-2020. Source: US FDA. Licensed CC0.

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