Henora REF: 70-4026-09V1 300psi I.V. Catheter Extension Set Product Usage: Catheter extension set for high pressure procedures.
Class I - Dangerous 🏥 Medical Devices
Recalled: March 28, 2014 RGI Medical Manufacturing Surgical Instruments
Nationwide
What Should You Do?
- Check if you have this product: Lot numbers 102131 and 110531.
- 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:
- RGI Medical Manufacturing, Inc.
- Reason for Recall:
- Problem with low adhesion of the tubing to luer connection which may lead to a separation of the extension set while in use.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
Henora REF: 70-4026-09V1 300psi I.V. Catheter Extension Set Product Usage: Catheter extension set for high pressure procedures.
Product Codes/Lot Numbers:
Lot numbers 102131 and 110531.
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-1996-2014