The appeal of the “M&C company” to Analytical Expertise Center of MOH of the Republic of Azerbaijan states that the medical device “Pencan 25gx3 1/2″ (88 mm) M. FK-EU/AP/SA”, produced by BBraun with the 23E24H8B05 series, recall from end users, retailers (pharmacies) and wholesalers (distributors) due to the risk of rupture during use of the part connecting the base of the needle and the steel cannula.
This appeal was investigated by employees of AEC of the MOH and, guided by the provisions of part 5 of the “Rules for the recall of medicines”, approved by Resolution of the Cabinet of Ministers of the Republic of Azerbaijan dated November 27, 2019 No. 460, the decision to recall the medical devices specified in the appeal was confirmed by the order of the Center.
Taking into account the above and the provisions of section 16 “Rule on the recall of medicines”, the import into the country, as well as the wholesale and retail sale of a medical device with the commercial name “Pencan 25gx3 1/2″ (88 mm) M. FK-EU/AP/SA released in series 23E24H8B05 is prohibited.
