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Quality Choice Autolet

CHAIN DRUG MARKETING ASSOCIATION, INC. · Model AT 0274QC · UDI-DI 00635515959347

QRL
10
510(k) clearances
238
Adverse events
1
Recalls
87
Facilities

Description

Quality Choice Autolet Lancing Device

Recalls

DateFirmReason
2025-07-25Home Health US, IncorporatedDue to incorrect/lack of Unique Device Identifier (UDI) codes.

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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.