# FDA recall Z-2774-2020

> **Smith & Nephew, Inc.** · Class II · device recall initiated 2020-07-16.

## Product

Tibial knee prosthesis

## Reason for recall

Due to an inconsistency in the raw material process, specific lots may contain units with internal non-homogenous material defects.

## Distribution

Domestic Distribution: AL, LA ,MN, KY, AR, MN, GA, TX, WI, NJ, NC, CT, NY, OH, IA, IN, NC, MA, SC, NV, CT, WV, NY, OH, MN, MI, SC, TN, FL, AZ, PA and MO.    International Distribution:   Austria, Belgium, China, Canada, Switzerland, Colombia, Cyprus, Check Republic, Denmark, Spain, France, Great Britain, Greece, Hungary, India, Italy, Lithuania, Mexico, Netherlands, Norway, Poland, Portugal, Romania, Serbia, Russia, Sweden, Slovenia, Turkey and Ukraine.

## Key facts

- **Recall number:** Z-2774-2020
- **Recalling firm:** Smith & Nephew, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2020-07-16
- **Report date:** 2020-08-19

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2774-2020

## Citation

> AI Analytics. FDA recall Z-2774-2020. Retrieved 2026-06-30 from https://api.ai-analytics.org/recall/Z-2774-2020. Source: US FDA. Licensed CC0.

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