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Conair
CONAIR CORPORATION · Model A31746UL · UDI-DI 00079642317463
3
510(k) clearances
84
Adverse events (3 deaths)
1
Recalls
132
Facilities
Description
Pill box
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2021-07-02 | Hero Health | Due to dispenser prompting for a missed dose that had already been dispensed |
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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.