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All product recalls associated with Abbott Laboratories Diagnostic Div.
Total Recalls
1000
Past Year
276
Class I (Serious)
242
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.
Unacceptable upward drift of results in control runs within 24 hour period.
Software may cause instrument to omit step causing reagent carrover which may effect patient test result
Software may cause instrument to omit step causing reagent carrover which may effect patient test result
Non-invasive blood pressure readings on central station may not match bedside monitor due to software anomaly.