This mdr is a consolidation of records summarized as part of the fda voluntary malfunction summary reporting program.1 device was not evaluated, as the issue was identified and resolved during a troubleshooting call between the customer and stryker technical support.50 devices were evaluated in the field and the issue was confirmed; 15 devices had worn components, 2 devices had cracked components, 4 devices had dirty components, 5 devices had bent components, 2 devices had an alignment issue, 1 device had a loose component, 3 devices had missing components, and 28 devices had broken/damaged components.The devices were repaired and returned.There was no remedial action taken.This device is not labeled for single use.
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