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On Call Stealth Lancing Device

Acon Laboratories, Inc. · Model G124-18A · UDI-DI 00682607541829

QRL
1
510(k) clearances
262
Adverse events
1
Recalls
86
Facilities

Description

1 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.