Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
BD PhoenixTM AP Recalled by Becton Dickinson & Co. Due to Potential unexpected movement of robot arm
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 & Co. directly.
Affected Products
BD PhoenixTM AP, Catalog Number 448010 The BD Phoenix" AP instrument is designed for use with the BD Phoenix" system is intended to standardize ID broth tube inoculum, add AST indicator to the AST broth tube and transfer an aliquot of ID broth to AST broth tubes, as required for preparing samples for use on the BD Phoenix" system, which performs identification and susceptibility testing
Quantity: 7 units
Why Was This Recalled?
Potential unexpected movement of robot arm
Where Was This Sold?
This product was distributed to 3 states: CA, NC, TN
About Becton Dickinson & Co.
Becton Dickinson & Co. has 183 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report