Cordis MAXI LD PTA Dilatation Catheter, for cardiovascular use.
Class I - DangerousWhat Should You Do?
- Check if you have this product: Catalog Number: 4171460S; Lot Number: 82169860; Expiry Date: 10/31/2020
- 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 Corporation
- Reason for Recall:
- Product was manufactured utilizing an expired inner body.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
Cordis MAXI LD PTA Dilatation Catheter, for cardiovascular use.
Product Codes/Lot Numbers:
Catalog Number: 4171460S; Lot Number: 82169860; Expiry Date: 10/31/2020
Distribution:
Distributed in: US, AL, AZ, FL, MN, MO
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-0250-2020
Related Recalls
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There is a potential for distal tip dislodgement or separation.
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There is a potential for distal tip dislodgement or separation.