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INBRIJA®
Merz Pharmaceuticals, LLC · Model Inbrija Device · UDI-DI 00310144300011
KCO
Prescription
1
510(k) clearances
48
Adverse events
1
Recalls
75
Facilities
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2022-06-23 | Family Dollar Stores, Llc. | Affected product was not appropriately stored in temperature-controlled areas between April 30, 2022 - June 10, 2022. |
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Get your free API keyRead the docsData 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.