Clinical safety

Recovrly is a UK-registered Class I medical device (Recovrly Health Ltd), intended to support users in preparation and rehabilitation pathways by providing access to clinician-created or clinician-approved informational content, exercise guidance, and basic health and wellbeing data capture and display.

Recovrly is not a diagnostic tool and does not replace your care team's advice, assessment or treatment. It's intended to support, not replace, healthcare professional judgement, clinical assessment, diagnosis, treatment, monitoring or advice.

If you have urgent or worsening symptoms, contact your care team, your GP, or emergency services immediately. Recovrly is not built or intended for emergencies.

Every clinical content item moves through author, draft, clinical review and approval before publishing, with a named owner, reviewer and scheduled re-review date. High-risk safety content gets shorter review intervals and stricter publishing permissions than low-risk lifestyle content.

_kim, Recovrly's supporting Bayesian network, is intended to support engagement with clinician-created pathways by suggesting or prioritising content that already exists within a user's predefined pathway. It does not generate new clinical content, create new exercises, alter clinical pathways, determine clinical suitability, diagnose, predict, monitor, treat, triage, escalate, or make clinical decisions.

Recovrly is developed under a formal risk management process aligned with ISO 14971, with a maintained risk management file.

If you experience or notice a safety issue while using Recovrly, contact support@recovrly.com as soon as possible.

Recovrly is classified as a Class I medical device under the UK Medical Devices Regulations 2002, as amended, self-declared by Recovrly Health Ltd (company number 17134638). See our evidence page for published research and active evaluations.