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All product recalls associated with BD Diagnostic Systems.
Total Recalls
1000
Past Year
1000
Class I (Serious)
145
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.
Febrile Antigens and Control Antisera that were released prior to August 2003 contained the 12/2000 revised insert that had incorrect testing instructions.
The internal speaker components are failing and do not produce an audio alarm in the event of patient emergency.
The internal speaker components are failing and do not produce an audio alarm in the event of patient emergency.