Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
BD Insyte Autoguard BC Recalled by Becton Dickinson Infusion Therapy Systems, Inc. Due to Catheters may contain a hole in the catheter...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Becton Dickinson Infusion Therapy Systems, Inc. directly.
Affected Products
BD Insyte Autoguard BC, Shielded IV Catheter with Blood Control Technology, REF: 382533, 20 GA x 1.00 in (1.1x25 mm) 63 mL/min, Rx Only. BD Insyte Autoguard BC Shielded IV Catheter is intended to be inserted into a patient's peripheral vascular system for short term use to sample blood, monitor blood pressure, or administer fluids.
Quantity: 26,400 units
Why Was This Recalled?
Catheters may contain a hole in the catheter tubing, which could result in leakage during the insertion process.
Where Was This Sold?
This product was distributed to 1 state: IL
About Becton Dickinson Infusion Therapy Systems, Inc.
Becton Dickinson Infusion Therapy Systems, Inc. has 11 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report