Fogarty Thru-Lumen Embolectomy Catheter, REF: 12TLW805F35
Class I - DangerousWhat Should You Do?
- Check if you have this product: UDI-DI: 00690103043532, Lot: 64936927
- 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:
- Edwards Lifesciences, LLC
- Reason for Recall:
- Inadvertent release of embolectomy catheters that may experience slower than normal balloon deflation (greater-than 15 seconds).
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- ongoing
Product Information
Full Description:
Fogarty Thru-Lumen Embolectomy Catheter, REF: 12TLW805F35
Product Codes/Lot Numbers:
UDI-DI: 00690103043532, Lot: 64936927
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-0238-2024
Related Recalls
due to complaints received for 3mm to 4mm section wire exposed/protruding from the outside of the cannula body.
due to complaints received for 3mm to 4mm section wire exposed/protruding from the outside of the cannula body.
due to complaints received for 3mm to 4mm section wire exposed/protruding from the outside of the cannula body.