---
title: "O.T.D - Optimum Traction Device - Street Orange. Single use traction splint. — FDA record Z-1395-2024 | Is It on Recall"
description: "Failure of adhesive to secure the pole insert."
url: https://isitonrecall.com/recall/fda-device-z-1395-2024-o-t-d-optimum-traction-device-street-orange-single-use-traction-splint/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# O.T.D - Optimum Traction Device - Street Orange. Single use traction splint. — FDA record Z-1395-2024

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Feb 27, 2024. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: O.T.D - Optimum Traction Device - Street Orange. Single use traction splint.
- **Reason**: Failure of adhesive to secure the pole insert.
- **Classification**: Class II
- **Recalling firm**: Emergency Products & Research
- **Quantity**: 190,000 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1395-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1395-2024%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | Model EP-800; Lot No. 20230523-04, 09082023-11, 09082023-12, 122023-3, 122023-2, 122023-1. |

Match all identifying details in the current notice. A brand name alone is not enough.

## 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.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

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## Dates in the source

- **Report date**: Apr 3, 2024
- **Recall initiation date**: Feb 27, 2024
- **Center classification date**: Mar 28, 2024

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1395-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Emergency Products & Research records](https://isitonrecall.com/brand/emergency-products-research/)