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All product recalls associated with Technomed Europe Amerikalaan 71 Maastricht-Airport Netherlands.
Total Recalls
3
Past Year
0
Class I (Serious)
0
Most Recent
Jul 2024
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.
Product has have presence of brown discoloration or substance on the hinge area of the device
Burns of varying degrees can occur to patients with electrodes left in while in the MRI scanner as a result of inadequate safety information in the IFU.
There is a high risk of the blue hub detaching from the corkscrew needle, resulting the the needle remaining in the patient's scalp.