---
title: "Soltive SuperPulsed Laser System Wireless Footswitch, Model TFL-AFSWL — FDA record Z-2506-2024 | Is It on Recall"
description: "Difficulties in pairing the wireless footswitch with the Soltive Laser, potentially delaying the surgical procedure."
url: https://isitonrecall.com/recall/fda-device-z-2506-2024-soltive-superpulsed-laser-system-wireless-footswitch-model-tfl-afswl/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Soltive SuperPulsed Laser System Wireless Footswitch, Model TFL-AFSWL — FDA record Z-2506-2024

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 May 31, 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**: Soltive SuperPulsed Laser System Wireless Footswitch, Model TFL-AFSWL
- **Reason**: Difficulties in pairing the wireless footswitch with the Soltive Laser, potentially delaying the surgical procedure.
- **Classification**: Class II
- **Recalling firm**: Olympus Corporation of the Americas
- **Quantity**: 1,838 Units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2506-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2506-2024%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: TFL-AFSWL; UDI-DI: 00821925044258; Serial Numbers: All Serial Numbers. |

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

## Distribution

Worldwide distribution - US Nationwide and the countries of Australia, Canada, Chile, Germany, Hong Kong, Japan, Singapore.

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

- [Alaska](https://isitonrecall.com/state/alaska/)
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- [Idaho](https://isitonrecall.com/state/idaho/)
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- [Oregon](https://isitonrecall.com/state/oregon/)
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- [Rhode Island](https://isitonrecall.com/state/rhode-island/)
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- [Utah](https://isitonrecall.com/state/utah/)
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- [West Virginia](https://isitonrecall.com/state/west-virginia/)
- [Wyoming](https://isitonrecall.com/state/wyoming/)

## Dates in the source

- **Report date**: Aug 14, 2024
- **Recall initiation date**: May 31, 2024
- **Center classification date**: Aug 5, 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-2506-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Olympus Corporation of the Americas records](https://isitonrecall.com/brand/olympus-corporation-of-the-americas/)