Recall issued for nitrofurantoin antibiotic due to packaging error

A recall has been issued for batches of nitrofurantoin, an antibiotic used for urinary tract infections, due to an extra tablet found in some packs. The issue is linked to the manufacturing process, not broken capsules. The Medicines and Healthcare products Regulatory Agency has asked suppliers to quarantine specific batch numbers distributed in December. Patients are advised to return affected packs to their pharmacies. While taking the extra tablet may have resulted in a higher dose, the agency states it should not cause harm. Patients experiencing side effects or concerns are encouraged to seek medical advice.