Venner Medical

06/01/2026

Developed by clinicians, for clinicians, WireSafe™ is the culmination of years of human-factors mapping and real-world validation

23/12/2025

Checklists, double-checks and supervision haven’t ended guidewire retention. WireSafe™ provides what is missing — A mechanical forcing function that demands guidewire removal. In line with 2025 guidance, WireSafe™ is the only engineered anti-retention system available.

12/12/2025

Hospitals must now demonstrate that they have ‘put in place all possible procedures to prevent retained guidewires.’ WireSafe™ is a proven, award-winning device, endorsed for innovation by NHS and AHSN networks and offers simple compliance with the new national guidance.

05/12/2025

PneuX system training for the NIHR multi centre protect airways trial is underway accross the UK and we are excited to start the recruitment of patients over the coming weeks..

01/12/2025

Last few 'free' places for Charities! email info@venner.com

01/12/2025

The Association of Anaesthetists Safe Vascular Access 2025 guidelines call for anti-retention devices. WireSafe™ — The only engineered solution — removes human error from the equation.

12/09/2025

For more information, visit https://www.venneracademy.com/

11/09/2023

Packaging that removes the possibility of human error.

21/08/2023

31/07/2023

Guide wire retention is classed as a never event in the UK and an adverse event in the US both nationally reportable incidents and classed as the 3rd most commonly retained foreign object. Reported as a 1 in 10 RFO occurrence by the California department of public health. “A serious incident that is wholly preventable” with a 1:3000⁴ occurrence and a 35% mortality rate³ occurring only through human error. A retained guidewire is a serious reportable event (SRE) and included in the national reporting and litigation system (NRLS) within NHS improvement.