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Twist Lancet

Shandong Lianfa Medical Plastic Products CO.,LTD · Model LF-TL-30 · UDI-DI 06949517004337

QRL
10
510(k) clearances
250
Adverse events
1
Recalls
87
Facilities

Description

Sterile Lancet for Single Use (Box of 150 lancets), Sterilized with Irradiation

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.