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Publix Autolet
PUBLIX SUPER MARKETS, INC. · Model AT 0274PX · UDI-DI 00041415031784
10
510(k) clearances
262
Adverse events
1
Recalls
86
Facilities
Description
Publix Autolet lancing device
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-07-25 | Home Health US, Incorporated | Due to incorrect/lack of Unique Device Identifier (UDI) codes. |
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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.