WHO Pharmaceuticals Newsletter 1998, No. 09&10
(1998; 23 pages)
Índice de contenido
Abrir esta carpeta y ver su contenidoRegulatory decisions
Abrir esta carpeta y ver su contenidoDrug surveillance
Abrir esta carpeta y ver su contenidoNew developments
Cerrar esta carpetaMedical devices
Ver el documentoBlood glucose meters - recalled because of error readings: USA
Ver el documentoEpiPen epinephrine auto-injectors - recall of syringes: Switzerland
Ver el documentoMedical devices - the year 2000 problem: guidance document: USA
Ver el documentoSkin wound closure adhesive - approved: USA
Ver el documentoWeight loss device - recalled: USA
Abrir esta carpeta y ver su contenidoGeneral information
Abrir esta carpeta y ver su contenidoMedication errors
Abrir esta carpeta y ver su contenidoVeterinary medicine
 

EpiPen epinephrine auto-injectors - recall of syringes: Switzerland

Switzerland. Following the alerts concerning the recall by the manufacturer, Meridian Medical Technologies Inc., of the EpiPen and the EpiPen Junior Autoinjectors because some 10% of units were found to be ineffective due to damage during the manufacturing process, the Intercantonal Office for the Control of Medicines has recalled the following batches:

EpiPen: 806 509, 725 902, 732 213
EpiPen Junior: 806 507, 725 901, 732 215.

Patients are advised to return immediately the defective syringes to their doctor or pharmacist and exchange them with new syringes. In the interim, patients are advised to used the syringes they have in an emergency.

[See also Pharmaceuticals Newsletter Nos. 7&8, July&August 1998]

Reference: Schweizer Apothekerzeitung, 16/98.

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Última actualización: le 3 mayo 2013