🔍 RecallPedia

BD Insyte Autoguard BC Shielded IV Catheter with Blood Control Technology 20GA X 1.00in, REF: 382533

Class I - Dangerous
🏥 Medical Devices Recalled: October 4, 2023 Becton Dickinson Infusion Therapy Systems Surgical Instruments Nationwide

What Should You Do?

  1. Check if you have this product:
    UDI-DI: 00382903825332, Lot: 3166524, Expiration: 2026/05/31
  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:
Over-the-needle, intravascular catheters may have needles that do not retract properly into the barrel, which could result in contaminated needlestick injury, blood leaking from the insertion site or catheter, and repeat catheter insertion attempts, due to catheter being inadvertently removed from the insertion site.
Classification:
Class I - Dangerous

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

Status:
ongoing

Product Information

Full Description:

BD Insyte Autoguard BC Shielded IV Catheter with Blood Control Technology 20GA X 1.00in, REF: 382533

Product Codes/Lot Numbers:

UDI-DI: 00382903825332, Lot: 3166524, Expiration: 2026/05/31

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0400-2024

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