Home/Recalls/UK-MHRA-devices-supplied-without-valid-ukca-slash-ce-conformity-markings-or-certification-remove-from-use-and-place-in-quarantine-dsi-slash-2026-slash-007
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Devices supplied without valid UKCA/CE conformity markings or certification: remove from use and place in quarantine (DSI/2026/007)

Published: August 10, 2026Recall ID: devices-supplied-without-valid-ukca-slash-ce-conformity-markings-or-certification-remove-from-use-and-place-in-quarantine-dsi-slash-2026-slash-007Category: devicesCountry: UK
UK
Medical DeviceUKUK

Devices supplied without valid UKCA/CE conformity markings or certification: remove from use and place in quarantine (DSI/2026/007)

Recalling Firm: MHRA

Reason for Recall / Hazard

The MHRA has become aware of a number of medical devices being supplied on the UK market that do not comply with the requirements of the UK Medical Device Regulations 2002 (UK MDR 2002) or with the EU...

Product Description & Identification

The MHRA has become aware of a number of medical devices being supplied on the UK market that do not comply with the requirements of the UK Medical Device Regulations 2002 (UK MDR 2002) or with the EU Medical Devices Regulat…

Affected Products

Devices supplied without valid UKCA/CE conformity markings or certification: remove from use and place in quarantine (DSI/2026/007)

Additional Source Details

FieldValue
Guidtag:www.gov.uk,2005:/drug-device-alerts/devices-supplied-without-valid-ukca-slash-ce-conformity-markings-or-certification-remove-from-use-and-place-in-quarantine-dsi-slash-2026-slash-007
Linkhttps://www.gov.uk/drug-device-alerts/devices-supplied-without-valid-ukca-slash-ce-conformity-markings-or-certification-remove-from-use-and-place-in-quarantine-dsi-slash-2026-slash-007
Pub Date2026-08-10T14:00:16+01:00
Extracted categorydevices

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Overview

  • Recalling FirmMHRA
  • Risk LevelMedical Device Alert
  • DistributionUnited Kingdom
Recall Hazard Severity
Caution (Class III)
Official Agency Alert

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