🔍 RecallPedia

MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Straight Extensions with IC Components: 12 Fr/Ch (4.0 mm) x 24 cm;

Class I - Dangerous
🏥 Medical Devices Recalled: October 17, 2025 Mozarc Medical US Surgical Instruments Nationwide

What Should You Do?

  1. Check if you have this product:
    REF Number: 8888102004HP; UDI-DI: (Individual unit) 10884521128002, (Carton) 20884521128009; Lot number: 2424500197;
  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:
Mozarc Medical US LLC
Reason for Recall:
A potential issue with the seal integrity of header bag packaging.
Classification:
Class I - Dangerous

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

Status:
ongoing

Product Information

Full Description:

MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Straight Extensions with IC Components: 12 Fr/Ch (4.0 mm) x 24 cm;

Product Codes/Lot Numbers:

REF Number: 8888102004HP; UDI-DI: (Individual unit) 10884521128002, (Carton) 20884521128009; Lot number: 2424500197;

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0425-2026

Related Recalls