ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 603014MC
Class I - DangerousWhat Should You Do?
- Check if you have this product: UDI/DI 20705032056790; Lot Numbers: 35265492
- 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:
- Cordis US Corp
- Reason for Recall:
- There is a potential for separation of the ANGIOGUARD RX / XP delivery system and capture sheath which include but are not limited to situations of an intra-procedural delay, unplanned percutaneous or surgical intervention, or stroke; while a replacement device is prepared.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- ongoing
Product Information
Full Description:
ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 603014MC
Product Codes/Lot Numbers:
UDI/DI 20705032056790; Lot Numbers: 35265492
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-1488-2023
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