Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
ETEST XM256 (Cefuroxime) Recalled by BioMerieux SA Due to Potential performance issues. False Susceptible result instead of...
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 SA directly.
Affected Products
ETEST XM256 (Cefuroxime), Foam: 506958-506918; SPB: 412304-412305 ETEST is a quantitative technique for determining the antimicrobial susceptibility of Gram-negative and Gram-positive aerobic bacterial such as Enterobacteriaceae, Pseudomonas, Staphylococcus and Enterococcus species and fastidious bacteria
Quantity: 7,160 units
Why Was This Recalled?
Potential performance issues. False Susceptible result instead of Intermediate and False Intermediate result with certain methods.
Where Was This Sold?
This product was distributed to 37 states: AZ, AR, CA, CT, DE, FL, GA, ID, IL, IN, IA, KY, LA, MD, MA, MI, MS, MO, NE, NH, NJ, NY, NC, ND, OH, OK, OR, PA, SC, SD, TN, TX, VA, WA, WV, WI, DC
About BioMerieux SA
BioMerieux SA has 45 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report