Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Lombart 90D Clear with case Visualization during diagnosis and laser Recalled by Volk Optical Inc Due to Mislabeling
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Volk Optical Inc directly.
Affected Products
Lombart 90D Clear with case Visualization during diagnosis and laser therapy of the human retina (fundus) using a slit lamp.
Quantity: 78 units
Why Was This Recalled?
Mislabeling. The incorrect lot number was engraved on the anodized aluminum ring. The correct lot number is BE03356; however, BD03356 was engraved on the ring in error.
Where Was This Sold?
This product was distributed to 1 state: VA
About Volk Optical Inc
Volk Optical Inc has 4 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report