FDA Device Intelligence
Home › Care Living Diagnostics Inc. › CareLiving Lancing Device+100 Lancets

CareLiving Lancing Device+100 Lancets

Care Living Diagnostics Inc. · Model Lancing Device+Lancets · UDI-DI 00383568100413

QRLQRK
1
510(k) clearances
250
Adverse events
1
Recalls
87
Facilities

Description

1 x CARELIVING Lancing device, 100 x 30 Gauge Lancets.1 x User Guide,LESS PAINFUL,STRONG PENETRATION,12 OPTIONAL DEPTH SETTINGS,EASY-TO-USE LANCET INJECTOR

Recalls

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

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
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.