MEDDEV Safety Signals

Evidence before conclusions.

MEDDEV reports turn public regulatory data into decision-ready safety signals. Every issue separates report volume from actual risk and states what the data cannot prove.

Issue 02 · 24 July 2026 · Swissmedic

Which medical devices appeared most often in safety notices?

An analysis of 250 field safety corrective action and recall publications: device groups, recurring classes, and the implications for manufacturers.

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Swissmedic publications

250Publications dated from 1 January through 30 June 2026.

Issue 01 · 24 July 2026 · FDA MAUDE

Medical Device Safety Signals: Q2 2026

An analysis of 923,518 reports received by FDA: event mix, device-category concentrations, recurring problem codes, and the implications for post-market surveillance.

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Reports received by FDA

923,518MAUDE reports received from 1 April through 30 June 2026.

MEDDEV reports do not replace a device-specific risk assessment. Raw report counts do not include an installed-base denominator, exposure duration, or complete reporting coverage.