The company Laboratori Baldacci Spa with email dated 27 November 2024, communicated, in its capacity as distributor, that it had ordered the withdrawal, for precautionary and voluntary purposes, of a batch of a decongestant spray medical device useful for clearing the nose in case of colds and allergies, sold in pharmacies but also via the internet. In detail, this is the medical device STERIMAR Nose sensitive to colds 100 ml distributed by the company Laboratori Baldacci Spa with registered office in Pisa in via S. Michele degli Scalzi, 73 but produced by the French company Sofibel Laboratoire Fumouze with headquarters in Levallois-Perret , in Rue Victor Hugo n 110-114. The lot affected by the recall is PH4065A with expiration of 03/31/2027, code paraf. 902235353.
The provision was adopted, notes Giovanni D’Agata, president of the “Rights Desk”, following a report received from the company Sofibel Laboratoire Fumouze, manufacturer of the device in question. Sterimar Cu Nasal Spray is a device for the physiological micro-diffusion of sea water for washing the nasal mucosa which purifies the nose and thins the mucus, to facilitate correct breathing. By virtue of this communication, Giovanni D’Agata, president of the “Rights Desk”, recommends that patients being treated with the device verify the batch number and, if it corresponds to the recalled one, to suspend its use.
