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All product recalls associated with ABX Diagnostics Inc.
Total Recalls
5
Past Year
0
Class I (Serious)
0
Most Recent
Mar 2006
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.
Labels can be incorrectly placed on a sample tube resulting in a possible error in results attributed to a sample.
Device can generate overestimated platelet results.
Power failure having impact on software.
Software defect, instrument may erroneously give a result of '0' or '---'.