FDA Device Intelligence
HomeB BRAUN INTERVENTIONAL SYSTEMS, INC › Voluminous™

Voluminous™

B BRAUN INTERVENTIONAL SYSTEMS, INC · Model 622513 · UDI-DI 04046964539022

MAVKOE Prescription
10
510(k) clearances
3,682
Adverse events (8 deaths)
29
Recalls
61
Facilities

Description

40CC-15ATM VOLUMINOUS INFLATION DEVICE

Recalls

DateFirmReason
2025-08-05Boston Scientific CorporationThe Encore 26 Inflation Device is used with balloon dilation catheters to create and monitor pressure in the balloon and to deflate the balloon. An internal investigation determine
2024-11-06Abbott Vascular IncInflation Device used during cardiovascular procedures may leak in the indeflator at the hose rotating luer or at the gauge, which could lead to air embolism.
2024-11-06Abbott Vascular IncInflation Device used during cardiovascular procedures may leak in the indeflator at the hose rotating luer or at the gauge, which could lead to air embolism.
2024-11-06Abbott Vascular IncInflation Device used during cardiovascular procedures may leak in the indeflator at the hose rotating luer or at the gauge, which could lead to air embolism.
2024-11-06Abbott Vascular IncInflation Device used during cardiovascular procedures may leak in the indeflator at the hose rotating luer or at the gauge, which could lead to air embolism.
2022-03-11Abbott VascularDue to an increase in complaint trend for leaks and intermittent/loose connections.
2022-03-11Abbott VascularDue to an increase in complaint trend for leaks and intermittent/loose connections.
2022-03-11Abbott VascularDue to an increase in complaint trend for leaks and intermittent/loose connections.
2022-03-11Abbott VascularDue to an increase in complaint trend for leaks and intermittent/loose connections.
2022-03-11Abbott VascularDue to an increase in complaint trend for leaks and intermittent/loose connections.

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.