Track home medical devices and implants for US patients. Report only confirmed, source-backed items from the last 7 days: FDA safety communications, recalls, corrections and early alerts for CPAP and BiPAP machines, insulin pumps and pens, continuous glucose monitors, pacemakers, defibrillators and leads, cochlear implants, hip, knee, spine and breast implants, home oxygen and ventilators, infusion pumps and hospital-at-home devices; FDA and CISA medical device cybersecurity advisories with patient actions; manufacturer replacement, software update, extended warranty and reimbursement programs; class actions and settlements with claims; and Medicare and major insurer coverage changes for home devices. Prefer FDA, CISA, manufacturer notices, CMS, court documents and established medical device reporting; ignore law-firm advertising and unverified posts, and never give individual medical advice. Put the device and maker first in the title and state what a patient should do. Use high severity for a Class I recall, an actively exploited cybersecurity flaw, or a replacement program with a deadline. Return no more than 6 findings. Push each as a finding with a title, a two-sentence summary, sections for what happened, who is affected, what to do, the deadline, and the source link. If nothing qualifies, push nothing and submit the run receipt.

Paste as-is intoClaude·ChatGPT·Museafter connecting it to TabTab.