Product Desc: Product Name: CLEARCUT SAFETY INTREPID SB,2.4 Model/Catalog Number: 8065772445 Software Version: N/A Product Description: Ophthalmic knife Component: N/A
Class I - DangerousWhat Should You Do?
- Check if you have this product: Model/Catalog Number: 8065772445; UDI-DI: 00380657724451; Lot numbers: 15V018, 15V019, 15V01A, 15V01C, 15V01D, 15V036, 15W7UE, 15W7UF, 15W7UH, 15W7UJ, 15W996, 15W997, 161960, 161961, 161962, 161963, 167PR0, 167PT9, 168NM5, 168NM6, 168NM7, 168NN9, 168NNA, 168NNC, 168YFW, 169KL0, 169KL1, 169KL2, 169KL3, 169KTC, 169KTE, 169KTH.
- 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 Desc: Product Name: CLEARCUT SAFETY INTREPID SB,2.4 Model/Catalog Number: 8065772445 Software Version: N/A Product Description: Ophthalmic knife Component: N/A
Product Codes/Lot Numbers:
Model/Catalog Number: 8065772445; UDI-DI: 00380657724451; Lot numbers: 15V018, 15V019, 15V01A, 15V01C, 15V01D, 15V036, 15W7UE, 15W7UF, 15W7UH, 15W7UJ, 15W996, 15W997, 161960, 161961, 161962, 161963, 167PR0, 167PT9, 168NM5, 168NM6, 168NM7, 168NN9, 168NNA, 168NNC, 168YFW, 169KL0, 169KL1, 169KL2, 169KL3, 169KTC, 169KTE, 169KTH.
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-2652-2024
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