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All product recalls associated with Diagnostica Stago, Inc..
Total Recalls
1000
Past Year
304
Class I (Serious)
34
Most Recent
Nov 2025
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.
Decrease in sensitivity ; This could result in a false negative result for patients with weak to moderate lupus anticoagulants.
Product mislabeled; outer container labeled with incorrect lot number.
If the user opens the instrument lid during decontamination, the cycle will stop but the timer will continue resulting in the user believing the instrument has been decontaminated when it has not been.