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All product recalls associated with Creganna Medical Devices Parkmore House Mweeloon Galway Ireland.
Total Recalls
1000
Past Year
582
Class I (Serious)
91
Most Recent
Dec 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.
Three lots of product may be labeled with an incorrect expiration day
Defective Delivery System
When an update to the A710 Clinician Programmer software application for the Intellis Neurostimulation System was released, the corresponding version of the A901 Communication Manager software application was not available for download.