---
title: "FRT250 - 4.0-6.4 CARTRIDGE. Component of the Fassier-Duval Telescopic IM System — FDA record Z-2941-2024 | Is It on Recall"
description: "During the assembly of the FRT250 cartridge assembly, an incorrect component was used. Specifically, the FRT240-HEX (2) was used instead of the FRT250-HEX."
url: https://isitonrecall.com/recall/fda-device-z-2941-2024-frt250-4-0-6-4-cartridge-component-of-the-fassier-duval-telescopic-im-system/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# FRT250 - 4.0-6.4 CARTRIDGE. Component of the Fassier-Duval Telescopic IM System — FDA record Z-2941-2024

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 Jul 4, 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**: FRT250 - 4.0-6.4 CARTRIDGE. Component of the Fassier-Duval Telescopic IM System
- **Reason**: During the assembly of the FRT250 cartridge assembly, an incorrect component was used. Specifically, the FRT240-HEX (2) was used instead of the FRT250-HEX.
- **Classification**: Class II
- **Recalling firm**: ORTHOPEDIATRICS CANADA ULC Dba PEGA MEDICAL
- **Quantity**: 6 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2941-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2941-2024%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 | Part Number FRT250; Lot Numbers: F281-04, F462-02 |

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

## Distribution

Worldwide - US Nationwide distribution in the state of Texas and the countries of United Arab Emirates, Brazil, Canada, Netherlands.

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**: Sep 4, 2024
- **Recall initiation date**: Jul 4, 2024
- **Center classification date**: Aug 29, 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-2941-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [ORTHOPEDIATRICS CANADA ULC Dba PEGA MEDICAL records](https://isitonrecall.com/brand/orthopediatrics-canada-ulc-dba-pega-medical/)
