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All product recalls associated with Homeocare Laboratories, Inc..
Total Recalls
1000
Past Year
206
Class I (Serious)
410
Most Recent
Jan 2026
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.
cGMP deviations
cGMP deviations
A software defect in the DxA Automation System may cause tests to be run on patient samples in tube types not compatible with the requested test, leading to erroneous patient results