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Lilly Together

ELI LILLY AND COMPANY · Model MA9135 ANDROID (Version 12) · UDI-DI 00300021174552

NXQLMD
2
510(k) clearances
7
Adverse events
1
Recalls
61
Facilities

Description

Software as a medical device (SaMD) for some Lilly medicines which provides access to medication reminders and customer support services; Operates on Android devices (various manufacturers)

Recalls

DateFirmReason
2006-08-02Eatonform IncCertain lots of packet components of the firm's Doc-U-Dose Prescription Management System are separating from the paper along the sealed seam at the bottom of the packets causing t

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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.