Egoropal

No. This product has been recalled due to: Routine FDA inspection revealed serious deficiencies in aseptic manufacturing processes; a high risk to product quality and patient safety was assessed for aseptically filled batches, which are solutions for injection (parenteral products). Potential effects: infections, complications after parenteral administration, lack of drug sterility.

Stop using the product immediately. Return it to the store for a full refund. If you consumed it and feel unwell, contact your doctor.

Affected batch numbers: 4400718, 4500766, 4501274, 4400293, 4400851, 4500598, 4500832, 4500892, 4501060, 4501376