Radial Artery Catheterization Set, 1) NA-04550-1A & 2) NA-04550-X1A, device permits access to the peripheral arterial circulation or to other small vessels.
Class I - DangerousWhat Should You Do?
- Check if you have this product: Lot Numbers: 1) 23F16H0859 & 2) 23F16J0547
- 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:
- Arrow International Inc
- Reason for Recall:
- Needle supplier indicated the presence of loose polypropylene foreign matter above release specification.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
Radial Artery Catheterization Set, 1) NA-04550-1A & 2) NA-04550-X1A, device permits access to the peripheral arterial circulation or to other small vessels.
Product Codes/Lot Numbers:
Lot Numbers: 1) 23F16H0859 & 2) 23F16J0547
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-0486-2018
Related Recalls
Reports have been received regarding open seals on the packaging.
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