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uk-mhraMedicines Recall

Class 4 Medicines Defect Notification: Sandoz Limited, Apixaban 2.5mg and 5mg Tablets, EL(26)A/17

Published: March 26, 2026Recall ID: class-4-medicines-defect-notification-sandoz-limited-apixaban-2-dot-5mg-and-5mg-tablets-el-26-a-slash-17Category: drugsCountry: UK
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PharmaceuticalUKUK

Class 4 Medicines Defect Notification: Sandoz Limited, Apixaban 2.5mg and 5mg Tablets, EL(26)A/17

Recalling Firm: Sandoz Limited

Reason for Recall / Hazard

Sandoz Ltd. have informed the MHRA that the Patient Information Leaflet included in specified batches of Apixaban does not contain up‑to‑date information....

Product Description & Identification

Sandoz Ltd. have informed the MHRA that the Patient Information Leaflet included in specified batches of Apixaban does not contain up‑to‑date information.

Affected Products

Class 4 Medicines Defect Notification: Sandoz Limited, Apixaban 2.5mg and 5mg Tablets, EL(26)A/17

Additional Source Details

FieldValue
Guidtag:www.gov.uk,2005:/drug-device-alerts/class-4-medicines-defect-notification-sandoz-limited-apixaban-2-dot-5mg-and-5mg-tablets-el-26-a-slash-17
Linkhttps://www.gov.uk/drug-device-alerts/class-4-medicines-defect-notification-sandoz-limited-apixaban-2-dot-5mg-and-5mg-tablets-el-26-a-slash-17
Pub Date2026-03-26T14:01:58+00:00
Extracted categorydrugs

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Overview

  • Recalling FirmSandoz Limited
  • Risk LevelMedicines Recall
  • DistributionUnited Kingdom
Recall Hazard Severity
Caution (Class III)
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🚨 SAFETY ALERT: Sandoz Limited - Class 4 Medicines Defect Notification: Sandoz Limited, Apixaban 2.5mg and 5mg Tablets, EL(26)A/17

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