On (b)(6), the lay user/patient contacted lifescan (lfs) alleging that her onetouch ultra2 meter was set to the wrong calcode.The complaint was classified based on customer care advocate (cca) documentation.The patient reported that the meter issue occurred one week prior to contacting lfs.The patient manages her diabetes with fixed insulin doses and denied making any changes to her usual diabetes management routine in response to the alleged issue.The patient reported that ¿1 to 2 days¿ after the issue occurred she developed symptoms of ¿lightheadedness, nausea, dizziness, tiredness, weakness and chest pains¿ however denied receiving any treatment.During troubleshooting the cca noted that when the patient was walked through changing the code, the issue was resolved.Product was replaced and requested back.This complaint is being reported because the patient reportedly developed signs and/or symptoms that meet lfs¿ criteria for a serious injury adverse event after the alleged product issue began.
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