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Flexima™ Nasobiliary Catheter

BOSTON SCIENTIFIC CORPORATION · Model M00540120 · UDI-DI 08714729337386

FGE Prescription
10
510(k) clearances
33,655
Adverse events (359 deaths)
450
Recalls
148
Facilities

Description

Nasobiliary Catheter

Recalls

DateFirmReason
2026-05-22W L Gore & Associates, Inc.10 mm diameter x 7 cm with transmural drainage holes (VSWVH1006) incorrectly labeled as 10 mm diameter x 10 cm length devices without transmural drainage holes (VSWVN1010).
2026-05-22W L Gore & Associates, Inc.10 mm diameter x 7 cm with transmural drainage holes (VSWVH1006) incorrectly labeled as 10 mm diameter x 10 cm length devices without transmural drainage holes (VSWVN1010).
2026-05-21Boston Scientific CorporationPotential sterile breach of the pouches in which devices are packaged.
2026-05-21Boston Scientific CorporationPotential sterile breach of the pouches in which devices are packaged.
2026-05-21Boston Scientific CorporationPotential sterile breach of the pouches in which devices are packaged.
2026-05-21Boston Scientific CorporationPotential sterile breach of the pouches in which devices are packaged.
2026-05-21Boston Scientific CorporationPotential sterile breach of the pouches in which devices are packaged.
2026-05-21Boston Scientific CorporationPotential sterile breach of the pouches in which devices are packaged.
2026-03-05Cook IncorporatedProducts from the affected device lots were labeled with expiration dates that exceed the true shelf life.
2025-08-28Boston Scientific CorporationThe product in incorrectly labeled. The label indicates that the skive hole should be above the balloon, while it is actually positioned below, and vice versa.

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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.