Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Becton Recalled by Becton Dickinson & Co. Due to Clinical diagnostic instrument may exhibit minor defects, which...
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
Becton, Dickinson and Company, BD MAX (tm) (6 channel) Instruments, Catalog number 441916, clinical diagnostic instrument.
Quantity: 86 Instruments
Why Was This Recalled?
Clinical diagnostic instrument may exhibit minor defects, which could lead to erroneous test results.
Where Was This Sold?
This product was distributed to 12 states: CT, FL, IL, KS, MD, MI, MO, NY, PA, RI, TX, WI
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