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.38 devices were evaluated in the field and the issue was confirmed; 20 devices had broken/damaged components, 2 devices had detached components, 1 device had a bent component, 13 devices had worn components, 2 devices had alignment issues, 1 device had a loos component and 1 device had a missing component.The devices were repaired and returned.There was no remedial action taken.This device is not labeled for single use.
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