# FDA recall Z-2624-2017

> **Smith & Nephew, Inc.** · Class II · device recall initiated 2017-05-30.

## Product

LEGION(R) FEM CONE IMPACTOR HEADS:  a) REF 71441976, ID 18MM  b) REF 71441977, ID 20MM  c) REF 71441978, ID 22MM

## Reason for recall

The incorrect Loctite adhesive was used to assemble the impactor heads.

## Distribution

US distribution to TN

## Key facts

- **Recall number:** Z-2624-2017
- **Recalling firm:** Smith & Nephew, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-05-30
- **Report date:** 2017-07-05
- **Termination date:** 2021-12-10

- **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-2624-2017

## Citation

> AI Analytics. FDA recall Z-2624-2017. Retrieved 2026-07-13 from https://api.ai-analytics.org/recall/Z-2624-2017. Source: US FDA. Licensed CC0.

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