Home › ARKRAY USA, INC. › TechLITE® Lancets, 28g
TechLITE® Lancets, 28g
ARKRAY USA, INC. · Model 880128 · UDI-DI 00015482880187
1
510(k) clearances
238
Adverse events
1
Recalls
87
Facilities
Description
TechLITE Lancets 28g 100's. The lancet is intended for capillary blood sampling.
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-07-25 | Home Health US, Incorporated | Due 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 docsData 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.
