Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
BD Intelliport Medication Management System Sensor The system is indicated Recalled by Becton Dickinson & Company Due to The sterility of the product cannot be assured....
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 & Company directly.
Affected Products
BD Intelliport Medication Management System Sensor The system is indicated for use by healthcare professionals in a hospital or medical center setting with patients who are receiving manually administered bolus intravenous injections as part of their care to facilitate documentation of the medications.
Quantity: 250 units
Why Was This Recalled?
The sterility of the product cannot be assured. This may result in increased risk of infection.
Where Was This Sold?
US Distribution to:California and Utah.
About Becton Dickinson & Company
Becton Dickinson & Company has 169 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report