Loading...
Loading...
All product recalls associated with Horiba Instruments, Inc dba Horiba Medical.
Total Recalls
1000
Past Year
433
Class I (Serious)
138
Most Recent
Dec 2025
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
HORIBA Medical is recalling the ABX PENTRA 400 Reagent Container because they do not always sit properly into the reagent rack. In low reagent level scenarios, this could lead to insufficient reagent volume being pipetted and could lead to incorrect results being reported without an alarm. The defect would result in a false high or false low results for HbA1c and false high results for magnes
During an investigation of label issuance and reconciliation at the firm's contract manufacturer it was discovered that 948 labels of Beachbody Extreme Nutrition Base Shake entered into Beachbody Extreme Nutrition Fuel Shot production. Therefore some bottles of Beachbody Extreme Nutrition Fuel Shot were labeled Beachbody Extreme Nutrition Base Shake.
Defective container: A customer complaint revealed the presence of a defective seal on the top of a Mucinex pouch