---
title: "SOLTIVE Pro SuperPulsed Laser (TFL-SLS ) — FDA record Z-1384-2024 | Is It on Recall"
description: "A non-compliant power cord may have been supplied in regions that do not utilize the Type B or Type E/F plug configurations."
url: https://isitonrecall.com/recall/fda-device-z-1384-2024-soltive-pro-superpulsed-laser-tfl-sls/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# SOLTIVE Pro SuperPulsed Laser (TFL-SLS ) — FDA record Z-1384-2024

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 Jan 29, 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 Pro SuperPulsed Laser (TFL-SLS )
- **Reason**: A non-compliant power cord may have been supplied in regions that do not utilize the Type B or Type E/F plug configurations.
- **Classification**: Class II
- **Recalling firm**: Olympus Corporation of the Americas
- **Quantity**: 17 Units (OUS Only)
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1384-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1384-2024%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 Number: TFL-SLS; UDI/DI: 00821925044135; All serial numbers. |

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

## Distribution

Domestic: OUS Only; International distribution in the states of Australia, Chile, Germany, Hong Kong, Japan, New Zealand and Singapore.

No US distribution state could be established from this record. Check the official notice.

## Dates in the source

- **Report date**: Apr 3, 2024
- **Recall initiation date**: Jan 29, 2024
- **Center classification date**: Mar 27, 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-1384-2024%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/)