Stingray" Guidewire, labeled as 300cm. intended to facilitate placement of balloon dilatation catheters or other intravascular devices during percutaneous transluminal coronary angioplasty (PTCA) and percutaneous transluminal angioplasty (PTA).
Class I - DangerousWhat Should You Do?
- Check if you have this product: Material Number (UPN) H749M3004A0, Batch Number 21558994, Expiration Date 11/30/2019
- 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:
- Boston Scientific Corporation
- Reason for Recall:
- A batch of 185cm Stingray Guidewires are incorrectly labeled as 300cm guidewires.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
Stingray" Guidewire, labeled as 300cm. intended to facilitate placement of balloon dilatation catheters or other intravascular devices during percutaneous transluminal coronary angioplasty (PTCA) and percutaneous transluminal angioplasty (PTA).
Product Codes/Lot Numbers:
Material Number (UPN) H749M3004A0, Batch Number 21558994, Expiration Date 11/30/2019
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-0852-2019
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