Product Name: 25+ TTL PLUS VPAK 20000CPM BWV Model/Catalog Number: 8065830077 Software Version: N/A Product Description: Standardized assemblage of components, which includes the valved trocar entry system, that interface with the CONSTELLATION Vision System. Component: N/A
Class I - DangerousWhat Should You Do?
- Check if you have this product: Model/Catalog Number: 8065830077; UDI-DI: 380658300777; Lot numbers: 16A6HT, 16A6HU, 16A6HV, 16FX1Y, 16FX20, 16FE93, 16HE6Y, 16HE70, 16HYEN, 16HYEP.
- 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:
- Alcon Research LLC
- Reason for Recall:
- Alcon has detected an increase in complaint reports related to sharpness for specific ClearCut Dual Bevel Sideport and A-OK Comeal/Scleral V-Lance Ophthalmic knives.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- ongoing
Product Information
Full Description:
Product Name: 25+ TTL PLUS VPAK 20000CPM BWV Model/Catalog Number: 8065830077 Software Version: N/A Product Description: Standardized assemblage of components, which includes the valved trocar entry system, that interface with the CONSTELLATION Vision System. Component: N/A
Product Codes/Lot Numbers:
Model/Catalog Number: 8065830077; UDI-DI: 380658300777; Lot numbers: 16A6HT, 16A6HU, 16A6HV, 16FX1Y, 16FX20, 16FE93, 16HE6Y, 16HE70, 16HYEN, 16HYEP.
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-2647-2024
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