FDA Device recall Z-2416-2024
SlideView VS200 slide viewer
- FDA Device
- Class II
- ongoing
- Published 2024-08-07
On 2024-08-07 the FDA classified a Class II recall of SlideView VS200 slide viewer by Evident Scientific, citing 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 h….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2416-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-07-22 |
| Published | 2024-08-07 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Evident Scientific |
| Distribution | n/a |
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.
Identifiers
| code_info | 65159 67105 67104 69153 67106 69154 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2416-2024%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.