# FDA recall Z-1102-2023

> **Wishbone Medical, Inc.** · Class II · device recall initiated 2023-01-04.

## Product

WishBone Medical Smart Correction Dual Joint Express Struts, external skeleton fixation device    Type         Part Number  XXS           10-702-080095-0  XS              10-702-095115-0  Short        10-702-115150-0  Medium    10-702-140200  Long          10-702-190300-0

## Reason for recall

Firm identified that user may be unable to adjust the length of the Smart Correction Dual Joint Express Struts due to the collar release pin backing out. This may lead to a delay in correction.

## Distribution

US Nationwide distribution in the state of South Carolina.

## Key facts

- **Recall number:** Z-1102-2023
- **Recalling firm:** Wishbone Medical, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-01-04
- **Report date:** 2023-02-15

- **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-1102-2023

## Citation

> AI Analytics. FDA recall Z-1102-2023. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-1102-2023. Source: US FDA. Licensed CC0.

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