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Apex

COMPASS HEALTH BRANDS CORP. · Model 70013 · UDI-DI 00076855700136

NXB
3
510(k) clearances
78
Adverse events (3 deaths)
1
Recalls
128
Facilities

Description

MediPlanner® II

Recalls

DateFirmReason
2021-07-02Hero HealthDue to dispenser prompting for a missed dose that had already been dispensed

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.