# FDA recall Z-1395-2024

> **Emergency Products & Research** · Class II · device recall initiated 2024-02-27.

## Product

O.T.D - Optimum Traction Device - Street Orange. Single use traction splint.

## Reason for recall

Failure of adhesive to secure the pole insert.

## Distribution

US Nationwide distribution in the states of CA, CO, FL, GA, IL, IN, KS, MA, MI, NJ, NY, OH, OK, PA, SC, TX, UT, VA, WA.

## Key facts

- **Recall number:** Z-1395-2024
- **Recalling firm:** Emergency Products & Research
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-02-27
- **Report date:** 2024-04-03

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Kent, OH, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1395-2024

## Citation

> AI Analytics. FDA recall Z-1395-2024. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-1395-2024. Source: US FDA. Licensed CC0.

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