Cordis POWERFLEX P3, PTA Dilation Catheter, REF 420-6020S
Class I - DangerousWhat Should You Do?
- Check if you have this product: Lot 82155955, Use by date 2021-06-30
- 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:
- Cordis is recalling one (1) lot of POWERFLEX P3 PTA Dilatation Catheter due to the potential for body/shaft voids in the proximal seal area.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
Cordis POWERFLEX P3, PTA Dilation Catheter, REF 420-6020S
Product Codes/Lot Numbers:
Lot 82155955, Use by date 2021-06-30
Distribution:
Distributed in: US, UK
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-1477-2020
Related Recalls
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Class I - Dangerous
There is a potential for distal tip dislodgement or separation.
Class I - Dangerous
There is a potential for distal tip dislodgement or separation.