DOSI-FLOW

LEVENTON SAU · Model L2590260-NF-US · UDI-DI 08436020769160

LDR Prescription

510(k) clearances

Adverse events

Recalls

Facilities

Description

Regulator Extension Set with Female Luer Connector, Flow Regulator, Needle-Free Injection Site, and Rotating Luer Lock Connector

Recalls

Date	Firm	Reason
2017-06-19	ConMed Corporation	Intravascular (I.V.) fluid administration sets are exhibiting inaccurate or inconsistent flow rates.
2011-04-15	ConMed Corporation	ConMed received 16 complaints for STAT 2 Pumpette devices for inaccurate flow rates and for leakage from the body of the compensating controller. The investigation of the complain
2011-04-15	ConMed Corporation	ConMed received 16 complaints for STAT 2 Pumpette devices for inaccurate flow rates and for leakage from the body of the compensating controller. The investigation of the complain
2011-04-15	ConMed Corporation	ConMed received complaints of some units exhibiting inaccurate or inconsistent flow rates. It was determined that certain units were assembled with an incorrect component which co
2011-03-11	Leventon S. A. U.	Leventon, S.A.U. Barcelona, Spain is recalling DOSI-FLOW REGULATOR, Part Number 259-0250, Lot Numbers 101444L and 101494L. Product has potential to leak.

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 key Read 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.