Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling
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 Biomerieux Inc directly.
Affected Products
bioMerieux Kit, USB HDW, BTA3D60-B-B.40, Clinical instrument software, USB update and mounting hardware-English, catalog number 411956 Software update for the clinical instrument which is most commonly used to isolate and recover specimens drawn from adult and older pediatric patients that are acutely ill with signs and symptoms suggestive of blood stream infection, which can be due to a variety of sources including lung, abdomen, urinary tract, endovascular, and skin.
Quantity: 205 kits
Why Was This Recalled?
The product may mislabel patient information on culture specimen bottles due to a software miscommunication.
Where Was This Sold?
This product was distributed to 19 states: AZ, AR, CA, FL, KS, LA, MD, MN, MT, NV, NY, NC, OR, PA, RI, SC, TX, VA, WA
About Biomerieux Inc
Biomerieux Inc has 368 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report