UK recalls one batch of Ramipril due to possible Amlodipine mix-up; check labels, return mismatched packs.

A UK recall has been issued for one batch of Ramipril 5mg Capsules (batch GR164099) after a packaging error may have caused some boxes to contain Amlodipine 5mg Tablets instead. The Medicines and Healthcare products Regulatory Agency advises patients to check their medication labels and blister strips, returning any mismatched packs to pharmacies. Both drugs treat high blood pressure, but taking Amlodipine by mistake could cause dizziness due to lower blood pressure. The error likely occurred during packaging at the shared manufacturing facility. The recall is precautionary, with no widespread harm reported. Patients experiencing side effects should seek medical advice.