FDA Device Intelligence
HomeTERUMO BCT, INC. › Vista ®

Vista ®

TERUMO BCT, INC. · Model 25201 · UDI-DI 05020583252011

MMH Prescription
0
510(k) clearances
1,034
Adverse events (9 deaths)
2
Recalls
45
Facilities

Description

Vista Information System, Version 4.2

Recalls

DateFirmReason
2018-04-25ConvaTec, IncIt was discovered that the stoma hole of one lots of the Esteem synergy Stomahesive Skin Barrier wafers is larger that the 7/8 inch / 22mm specified on the box label.
2010-06-22SCC Soft ComputerSCC Soft Computer is issuing a Correction for SoftBank II Versions: 23.1.2.x, 23.2.0.x, and 25.0.0.x software applications. Functionality issue - For clients generating patient hi

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.