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HomeLemaitre Vascular, Inc. › Polyurethane Dual Lumen Occlusion Catheter

Polyurethane Dual Lumen Occlusion Catheter

Lemaitre Vascular, Inc. · Model 4F-2L-40 · UDI-DI 00840663102259

DQT Prescription
1
510(k) clearances
153
Adverse events (9 deaths)
4
Recalls
5
Facilities

Description

Polyurethane Dual Lumen Occlusion Catheter, 4F, 40cm

Recalls

DateFirmReason
2025-04-11LeMaitre Vascular, Inc.During internal product testing, it was observed that some packages to have incomplete seals (sterile barrier).
2013-10-21Medtronic VascularPotential for PTFE (polytetrafluroethylene) coating to delaminate and detach from Guidewire.
2013-10-21Medtronic VascularPotential for PTFE (polytetrafluroethylene) coating to delaminate and detach from Guidewire.
2005-05-17LeMaitre Vascular, Inc.LeMaitre Vascular is recalling certain lots of its Pruitt Aortic Occlusion Catheters due to a packaging defect which could compromise product sterility.

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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.