🔍 RecallPedia

REF: 381434 BD Insyte Autoguard Shielded IV Catheter, 20 GA x 1.16 in (1.1 x 30 mm) 60 mL/min, STERILEEO, RxOnly

Class I - Dangerous
🏥 Medical Devices Recalled: May 21, 2025 Becton Dickinson Infusion Therapy Systems Surgical Instruments Nationwide

What Should You Do?

  1. Check if you have this product:
    Lot# 4116814/ UDI: 00382903814343
  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:
Becton Dickinson Infusion Therapy Systems, Inc.
Reason for Recall:
Due to customer complaints, there is the possibility that catheter needle may be slow to retract or fail to retract.
Classification:
Class I - Dangerous

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

Status:
ongoing

Product Information

Full Description:

REF: 381434 BD Insyte Autoguard Shielded IV Catheter, 20 GA x 1.16 in (1.1 x 30 mm) 60 mL/min, STERILEEO, RxOnly

Product Codes/Lot Numbers:

Lot# 4116814/ UDI: 00382903814343

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-2007-2025

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