🔍 RecallPedia

High Pressure Tubing: REF: 502211002, HP9720E/C, HP9721E/C

Class I - Dangerous
🏥 Medical Devices Recalled: June 5, 2025 Merit Medical Systems Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    REF/UDI-DI/Lot(Expiration): 502211002/I3116954(8/16/2028); HP9720E/C/00884450859889/I3116059(12/10/2027), I3127321(12/30/2027), I3137220(1/28/2028); HP9721E/C/00884450859896/I3116060(12/10/2027)
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. 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:
Merit Medical Systems, Inc.
Reason for Recall:
High pressure tubing may relax over time causing it to partially separate from the connector resulting in a void that can trap air in the line. Use of the affected product may result in the trapped air being introduced into the patient.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
ongoing

Product Information

Full Description:

High Pressure Tubing: REF: 502211002, HP9720E/C, HP9721E/C

Product Codes/Lot Numbers:

REF/UDI-DI/Lot(Expiration): 502211002/I3116954(8/16/2028); HP9720E/C/00884450859889/I3116059(12/10/2027), I3127321(12/30/2027), I3137220(1/28/2028); HP9721E/C/00884450859896/I3116060(12/10/2027)

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-2293-2025

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