This mdr is a consolidation of records summarized as part of the fda voluntary malfunction summary reporting program.19 devices were evaluated in the field and the issue was confirmed; 18 units had broken/damaged components and 1 had a stuck component.The devices were repaired and returned.4 devices were not evaluated, as the issue was identified and resolved during a troubleshooting call between the customer and stryker technical support.There was no remedial action taken.This device is not labeled for single use.
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