FDAClass IIAugust 7, 2024

SlideView VS200 slide viewer recall

SlideView VS200 slide viewer,

Why was SlideView VS200 slide viewer recalled?

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.

What should I do if I have this product?

The recall is ongoing. Follow the firm and FDA instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

65159 67105 67104 69153 67106 69154

Product
SlideView VS200 slide viewer,
Recalling firm
EVIDENT SCIENTIFIC INC
Quantity
N/A
Distribution
US
Recall date
August 7, 2024
Classification
Class II
Status
Ongoing
Agency
FDA (device)
Open FDA enforcement record Latest recalls