Egoropal

No. This product has been recalled due to: A routine FDA inspection revealed serious deficiencies in aseptic manufacturing processes; the assessed risk to product quality and patient safety for aseptically filled batches on the market is high. The product is a solution for injection (parenteral product). Potential effects: infections, poisoning, severe complications after parenteral administration, lack of therapeutic efficacy.

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