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All product recalls associated with Synthes USA (HQ), Inc..
Total Recalls
1000
Past Year
593
Class I (Serious)
65
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.
The recalling firm has determined that the customized plates instruments do not have a cleared premarket notification.
The device has a software error that could potentially lead to a misdiagnosis.
Incorrect result: An intermittent low result may be seen with the last test run from an aliquot on a Dimension Vista System when connected to a StreamLAB Analytical Workcell. The sample delivery sequence may deliver insufficient surplus volume to the low sensitivity aliquot (second aliquot). The surplus sample volume is occasionally insufficient to and can cause short sampling on the last test.