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Twist Lancet (23G)

Shandong Lianfa Medical Plastic Products CO.,LTD · Model LF-TL-23 · UDI-DI 06949517002012

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

Description

Sterile Lancet for Single Use (Bag of 30 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.