This record is a consolidation of records summarized as part of the fda voluntary malfunction summary reporting program.1 device was functionally/visually inspected in the field.The device was repaired and returned to use.1 device was not evaluated, as a probable cause for the issue was identified during a troubleshooting call between the customer and stryker technical support 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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