Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
PREMIER EHEC and PREMIER EHEC Bulk. Recalled by Meridian Bioscience Inc Due to Internal testing has demonstrated that the indicated kit...
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 Meridian Bioscience Inc directly.
Affected Products
PREMIER EHEC and PREMIER EHEC Bulk.
Quantity: 4,747 EHEC + 180 EHEC Bulk
Why Was This Recalled?
Internal testing has demonstrated that the indicated kit lots produce false positive results when tested with some broth specimens.
Where Was This Sold?
This product was distributed to 38 states: AL, AZ, CA, CO, CT, FL, GA, ID, IL, IN, IA, KS, KY, LA, MD, MA, MI, MS, MO, MT, NE, NV, NJ, NY, NC, OH, OK, PA, SC, SD, TN, TX, UT, VT, VA, WA, WI, WY
About Meridian Bioscience Inc
Meridian Bioscience Inc has 15 total recalls tracked by RecallDetector.
Related Recalls
EndoVive Safety PEG Kit Recalled by Boston Scientific Corporation Due to Recall of kits which utilized ChloraPrep Triple Swabsticks...
Boston Scientific Corporation · February 10, 2026
Owner's Booklets and Instructions for Use that are used with Recalled by Trividia Health, Inc. Due to The system labeling (user manual and online labeling)...
Trividia Health, Inc. · February 6, 2026
Artelon FlexBand Dynamic Matrix Ref: 31057 Recalled by International Life Sciences Due to Augmentation devices failed bacterial endotoxin testing.
International Life Sciences · February 6, 2026
Owner's Booklets and Instructions for Use that are used with Recalled by Trividia Health, Inc. Due to The system labeling (user manual and online labeling)...
Trividia Health, Inc. · February 6, 2026
Owner's Booklets and Instructions for Use that are used with Recalled by Trividia Health, Inc. Due to The system labeling (user manual and online labeling)...
Trividia Health, Inc. · February 6, 2026
Data sourced from the FDA (Device). Last updated March 26, 2026. View original report