Go Backs
HomeCategoriesStatesCheck Your Home
Go Backs

Track product recalls and safety alerts from CPSC, FDA, NHTSA, and USDA. Stay informed and keep your family safe.

Browse

  • Categories
  • States
  • Check Your Home
  • Risk Levels

Agencies

  • CPSC
  • FDA Food
  • FDA Drug
  • FDA Device
  • FDA Veterinary
  • NHTSA
  • USDA

Company

  • About
  • FAQ
  • Contact
  • Terms of Service
  • Privacy Policy
Buy Me a Coffee

Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

ยฉ 2026 Go Backs. All rights reserved.

Medium RiskFDA Device
Medical Devices/Surgical Equipment

Introcan Safety 3 Closed IV Catheters Recalled for Valve Detachment Risk

Agency Publication Date: March 19, 2025
Share:
Sign in to monitor this recall

Summary

B Braun Medical Inc. is recalling 28,200 units of its Introcan Safety 3 Closed IV Catheter due to a manufacturing defect where the valve housing may detach. This defect leads to fluid leakage during use, which can interrupt medical procedures or expose caregivers to fluids. The recall specifically affects the 22 Ga. x 1 in. Purple Winged model (Model 4251128-02) from lot 24F09G8952.

Risk

The valve housing can detach from the catheter body, resulting in leakage of blood or medication. While no injuries have been reported, this failure can delay necessary medical treatment or increase the risk of healthcare worker exposure to patient blood.

What You Should Do

  1. This recall affects Introcan Safety 3 Closed IV Catheters (22 Ga. x 1 in., PUR, Winged) identified by model number 4251128-02 and UDI-DI 04046964014017.
  2. Identify affected products by checking for lot number 24F09G8952 printed on the individual product packaging or shipping carton.
  3. Stop using the recalled product. Contact the manufacturer or your distributor to arrange return, replacement, or correction.
  4. Call the FDA at 1-888-463-6332 (1-888-INFO-FDA) for additional information regarding this recall.

Your Remedy Options

๐Ÿ“‹Other Action

Manufacturer return and correction

How to: Stop using the recalled product. Contact the manufacturer or your distributor to arrange return, replacement, or correction.

Affected Products

Product: Introcan Safety 3 Closed IV Catheter (22 Ga. x 1 in., PUR, Winged)
Variants: 22 Ga. x 1 in., PUR, Winged
Model / REF:
4251128-02
Lot Numbers:
24F09G8952
UDI:
04046964014017

Passive safety IV catheter.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 96293
Status: Active
Manufacturer: B Braun Medical Inc
Sold By: hospitals; medical supply distributors
Manufactured In: United States
Units Affected: 28,200 units
Distributed To: California, Florida, Georgia, Illinois, Indiana, Maryland, Minnesota, Missouri, North Carolina, New Mexico, New York, Pennsylvania, Tennessee, Texas, Virginia, Washington

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.