Teva Israel Ltd. has expanded its recall of Nutrilon infant formula products after laboratory tests found elevated levels of the cereulide toxin in specific batches. The recall affects Nutrilon AR 900g and 400g products intended for infants with reflux, following a notice from the European manufacturer and recent international recalls due to the same toxin. The Ministry of Health instructed further testing, which confirmed that batch number 2026.12.01 exceeded safety thresholds established by authorities in Ireland and adopted in Israel. Consumers are advised not to use products from the affected batches, as cereulide can cause gastrointestinal symptoms in infants. For further information, customers are encouraged to contact the Nutrilon Consumer Service Center.