FDA Device Intelligence
Home › THROMBOLEX, INC. › Bashir™ S-B Endovascular Catheter 7Fr, 10.0cm basket

Bashir™ S-B Endovascular Catheter 7Fr, 10.0cm basket

THROMBOLEX, INC. · Model 7101 · UDI-DI 00850005115021

QEYKRA Prescription
10
510(k) clearances
31
Adverse events (4 deaths)
4
Recalls
23
Facilities

Description

Bashir™ S-B Endovascular Catheter 7Fr, 10.0cm basket

Recalls

DateFirmReason
2023-11-06Merit Medical Systems, Inc.The sterility of microcatheter and infusion system devices cannot be guaranteed.
2022-10-13Boston Scientific CorporationConsoles were shipped without an instruction for use (IFU) or with the incorrect IFU.
2022-05-25Boston Scientific CorporationProduct may be mislabeled.
2022-05-25Boston Scientific CorporationProduct may be mislabeled.

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 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.