The Recall Desk
HighFDA (Devices)·Z-2416-2024·Announced 2024-08-07

SlideView VS200 slide viewer laser shutter malfunction recall

The SlideView VS200 slide viewer has a broken laser fuse caused by a short circuit from a poorly positioned cable. This prevents the shutter from operating properly, leaving it stuck in an open or closed position.

What this means for you

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

Our severity reasoning: FDA Class II recall of a medical device with a laser safety-related component (shutter control) that cannot be operated due to electrical failure. No injuries have been reported, but the malfunction poses a potential risk of uncontrolled laser exposure if the shutter remains stuck open.

Plain-English summary

The SlideView VS200 slide viewer is being recalled due to a broken laser fuse caused by a short circuit inside the device. The short circuit results from a badly positioned cable that contacts the housing and frame, which destroys the laser fuse.

Once the fuse is destroyed, the device's shutter cannot be operated and remains stuck in its last position—either fully open or fully closed. This prevents proper operation of the device and poses a potential safety concern if the shutter is stuck open.

EVIDENT SCIENTIFIC INC is recalling the affected SlideView VS200 units. Customers who have this device should contact the manufacturer for repair or replacement instructions.

The recalled product

Product
SlideView VS200 slide viewer,
Manufacturer
EVIDENT SCIENTIFIC INC
Category
Medical Device — Laboratory Equipment
Hazard
  • electrical-short-circuit
  • shutter-malfunction
  • laser-safety

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (1)

  • 65159 67105 67104 69153 67106 69154

Distribution

Distribution scope not specified by the agency.

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