Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
PrepStain AG. For use in the screening and detection of cervical cancer. Recalled by Becton Dickinson & Co. Due to PrepStain system rack setting was incorrectly entered on...
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
PrepStain AG. For use in the screening and detection of cervical cancer.
Quantity: 890 instruments
Why Was This Recalled?
PrepStain system rack setting was incorrectly entered on one PrepStain system during a routine preventive maintenance visit by a BD Field Service Representative.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
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