# FDA recall Z-0572-2020

> **Wright Medical Technology, Inc.** · Class II · device recall initiated 2016-11-08.

## Product

SWANSON TRAPEZIUM IMPLANT, Part Number 4520002

## Reason for recall

The firm discovered a lack of adequate documentation confirming sterility on certain products.

## Distribution

US and Norway, Italy, Germany, France, South Africa, UK, Taiwan, Austria, Japan, Turkey, Denmark, Canada, Switzerland, Belgium, The Netherlands, Spain

## Key facts

- **Recall number:** Z-0572-2020
- **Recalling firm:** Wright Medical Technology, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2016-11-08
- **Report date:** 2019-12-04
- **Termination date:** 2020-11-03

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Arlington, TN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0572-2020

## Citation

> AI Analytics. FDA recall Z-0572-2020. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-0572-2020. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*
