# FDA recall Z-1808-2024

> **Wishbone Medical, Inc.** · Class II · device recall initiated 2024-04-05.

## Product

WishFIX Growth Control Plating System, Model Number: TEFCS28-080US. Orthopedic device.

## Reason for recall

The products in this lot are incorrectly packed with a Stainless-Steel implant instead of a Titanium implant as the packaging and part number indicated.

## Distribution

US distribution to Florida, New Jersey and Connecticut.

## Key facts

- **Recall number:** Z-1808-2024
- **Recalling firm:** Wishbone Medical, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-04-05
- **Report date:** 2024-05-22

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Warsaw, IN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1808-2024

## Citation

> AI Analytics. FDA recall Z-1808-2024. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-1808-2024. Source: US FDA. Licensed CC0.

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