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Puriblood

PURIBLOOD MEDICAL CO., LTD. · Model LRW-50-01-PS · UDI-DI 04719878520461

KSR
10
510(k) clearances
615
Adverse events (8 deaths)
4
Recalls
32
Facilities

Recalls

DateFirmReason
2012-01-20DeRoyal Industries IncDevice's needle may become dislodged from the cup during shipment or during use.
2012-01-20DeRoyal Industries IncDevice's needle may become dislodged from the cup during shipment or during use.
2006-06-21Becton Dickinson & CompanyFirm received complaints indicating failure of the Non-Patient (NP) sleeve to function properly. This sleeve covers the cannula and prevents leakage during blood collection.
2005-12-01Becton Dickinson & CompanyCracked finger grip luer adapter components on the Push Button Blood Collection Set.

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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.