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All product recalls associated with Disetronic Medical Systems, Inc..
Total Recalls
14
Past Year
0
Class I (Serious)
0
Most Recent
Apr 2009
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 "up" and "down" buttons, which are used for changing the program in the menu or to administer additional insulin through a bolus delivery, may experience intermittent failure or completely cease to operate.
The battery may turn the pump off without warning due to a design change in the battery.
The luer tube may break at the lock-tubing connection to the pump, causing an interruption of insulin delivery, which can and has contributed to hyperglycemia