Crescent Pharma Recalls Ramipril Capsules Over Packaging Error; Patients Advised to Check Medication

April 21, 2026
Crescent Pharma Recalls Ramipril Capsules Over Packaging Error; Patients Advised to Check Medication
  • A batch of Ramipril 10mg capsules from Crescent Pharma Limited is being recalled due to a possible manufacturing error that could mean some cartons contain 5mg blister strips inside 10mg packaging.

  • The risk to patients from brief exposure to the lower 5mg dose is very low, and any potential harm would likely develop gradually rather than immediately.

  • If a carton contains 5mg blister strips, patients should contact their dispensing pharmacy and follow guidance; if the carton is correctly labeled as 10mg, no action is required.

  • Editors should note the MHRA recall notice, reiterate the regulator’s role in the UK medicines system, and include media contact details.

  • Regulatory and safety communications emphasize monitoring for adverse effects and removing affected products from supply to protect patients, while acknowledging the low risk from brief exposure to a lower dose.

  • This is a Class 2 recall affecting patients, pharmacies, and wholesalers, with instructions for healthcare professionals to stop supplying the batch, quarantine remaining stock, and return it to the supplier.

  • The recall is classified as a Class 2 Patient, Pharmacy and Wholesaler recall, requiring halt of supply, quarantine of remaining stock, and return to the supplier.

  • Ramipril is used to treat high blood pressure, heart failure, and to reduce the risk of stroke, heart attack, and kidney problems after a heart event by widening blood vessels.

  • Pharmacy professionals should identify and contact all patients who received the impacted product, prioritizing the most recently dispensed ones, to confirm if they have stock to return.

  • Pharmacists should reach out to patients dispensed the product, focusing on those in the last 28 days, and advise them to check packaging for correct medication.

  • MHRA advises stopping supply of the affected batch and returning remaining stock; patients should seek medical advice if they’ve taken the wrong dose and report adverse reactions via the Yellow Card scheme.

  • Adverse reactions should be reported through the MHRA Yellow Card scheme.

Summary based on 4 sources


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