The Medicines and Healthcare merchandise Regulatory Company has introduced a recall
Ramipril 10 mg Capsules – Batch GR174091 Outer carton and BN/Exp Date data (Picture: MHRA)
Must know: Pressing recall of Ramipril blood strain medicine on account of packaging mix-up
- The Medicines and Healthcare merchandise Regulatory Company has issued an pressing recall for Ramipril 10mg Capsules after a severe packaging error was found.
- Crescent Pharma Restricted is recalling batch GR174091 after discovering that some cartons labelled as containing 10mg capsules really contained 5mg capsules as an alternative. The MHRA stated on Monday: “Crescent Pharma Restricted has acquired one grievance to this point, the place it has been recognized that, inside a sealed carton of Ramipril 10 mg Capsules Batch No.: GR174091, one blister pack of Ramipril 5 mg Capsules Batch No.: GR164094 was discovered.”
- Healthcare professionals have been instructed to right away cease supplying the affected batch and quarantine all remaining inventory. Pharmacies should contact sufferers who acquired the medicine between 13 Might 2025 and 16 April 2026.
- Sufferers prescribed Ramipril 10mg ought to test their medicine packaging for batch quantity GR174091. The MHRA suggested: “If the carton accommodates blister strips which can be labelled and comprise Ramipril 5 mg capsule, contact your meting out pharmacy within the first occasion.”
- Each medicine strengths deal with hypertension, coronary heart failure and kidney illness, with the MHRA noting that any results from decreased dosage could be gradual reasonably than life-threatening. Sufferers with issues ought to contact their pharmacy or GP instantly.
- Anybody experiencing adversarial reactions ought to report them by way of the MHRA Yellow Card scheme.
READ THE FULL STORY: Pressing new Ramipril blood strain medicine alert as sufferers ought to ‘contact pharmacy’
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