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🚨 Inspire Implant Recall Legal Trouble 🚨 The Inspire Sleep Apnea implant is under fire on two fronts: ⚠️ FDA Class I Recall (most serious) • Device: Inspire IV (Model 3028) • Issue: electrical leakage → device malfunction • Risks: painful shocks, loss of therapy, rapid battery drain, possible revision surgery • 32 devices flagged so far (no deaths reported) ⚖️ Legal Investigations • DOJ probe into Inspire’s marketing & reimbursement practices (False Claims / Anti-Kickback) • Investor lawsuits
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