Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
VersaTREK Instrument Series 240 REF 6240 Recalled by Remel Inc Due to Use of the recalled product may result in...
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 Remel Inc directly.
Affected Products
VersaTREK Instrument Series 240 REF 6240, Manufactured for Remel Inc. The VersaTREK System is for cultivating and recovering microorganisms, especially bacteria and yeasts, from blood and other normally sterile bodily fluids.
Quantity: 143 devices
Why Was This Recalled?
Use of the recalled product may result in false positive reports.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Remel Inc
Remel Inc has 70 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report