---
title: "SlideView VS200 slide viewer, — FDA record Z-2416-2024 | Is It on Recall"
description: "A broken fuse inside the laser that was caused by a short circuit at PIN 4 of the DOOR CTRL. This short circuit was caused by a badly positioned cable that made"
url: https://isitonrecall.com/recall/fda-device-z-2416-2024-slideview-vs200-slide-viewer/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# SlideView VS200 slide viewer, — FDA record Z-2416-2024

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 22, 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**: SlideView VS200 slide viewer,
- **Reason**: A broken fuse inside the laser that was caused by a short circuit at PIN 4 of the DOOR CTRL. This short circuit was caused by a badly positioned cable that made contact with the housing/frame and caused a short circuit and destroyed the fuse in the laser. This caused the shutter to remain in its most recent state; either in an open or closed position. Once the fuse was destroyed the shutter could not be operated.
- **Classification**: Class II
- **Recalling firm**: EVIDENT SCIENTIFIC INC
- **Quantity**: N/A
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2416-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2416-2024%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 | 65159 67105 67104 69153 67106 69154 |

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

## Distribution

US

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

## Dates in the source

- **Report date**: Aug 7, 2024
- **Recall initiation date**: Jul 22, 2024
- **Center classification date**: Jul 26, 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-2416-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [EVIDENT SCIENTIFIC INC records](https://isitonrecall.com/brand/evident-scientific-inc/)