20 Diopter Binocular Indirect Ophthalmoscope (BIO) Lens For visualization during diagnosis and laser therapy of the human retina (fundus) using a binocular indirect ophthalmoscope.
Class I - DangerousWhat Should You Do?
- Check if you have this product: Product Code: V20LC; Lot/Serial Numbers: BB09213 & BB09205
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- Volk Optical Inc
- Reason for Recall:
- The defect was with mis-engraving of the lot # directly on the product and its packaging. Mixed up device engraving of V20LC (lot # BB09213) with that from V60C (lot # BB09205).
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
20 Diopter Binocular Indirect Ophthalmoscope (BIO) Lens For visualization during diagnosis and laser therapy of the human retina (fundus) using a binocular indirect ophthalmoscope.
Product Codes/Lot Numbers:
Product Code: V20LC; Lot/Serial Numbers: BB09213 & BB09205
Distribution:
Distributed in: AZ, CA, GA, MN, NJ, NM
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-0966-2013
Related Recalls
The firm discovered that the incorrect lot number was engraved on the product.
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.
Mislabeling. The incorrect lot number was engraved on the anodized aluminum ring.