This record is a consolidation of records summarized as part of the fda voluntary malfunction summary reporting program.6 devices were functionally/visually inspected in the field.The devices were repaired and returned to use.1 device was not evaluated and no cause was determined, as the customer did not make the device accessible for testing.1 device was not evaluated, as a probable cause for the issue was identified though analysis of data between the customer information and stryker and no further assistance was requested by the customer.There was no remedial action taken.This device is not labeled for single use.
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