Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
PREVI Isola System Recalled by Biomerieux Inc Due to The instrument may not dispense the specimen onto...
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
PREVI Isola System, Catalog numbers 29500 and 29500R, bioMerieux, Inc., Durham, NC. Intended to perform the inoculation and streaking of Prepoured Media (PPM) with liquid microbiological samples.
Quantity: 350 systems
Why Was This Recalled?
The instrument may not dispense the specimen onto the pre-poured media resulting in a false negative result.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
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