WHO Pharmaceuticals Newsletter 1998, No. 09&10
(1998; 23 pages)
Table of Contents
Open this folder and view contentsRegulatory decisions
Open this folder and view contentsDrug surveillance
Open this folder and view contentsNew developments
Close this folderMedical devices
View the documentBlood glucose meters - recalled because of error readings: USA
View the documentEpiPen epinephrine auto-injectors - recall of syringes: Switzerland
View the documentMedical devices - the year 2000 problem: guidance document: USA
View the documentSkin wound closure adhesive - approved: USA
View the documentWeight loss device - recalled: USA
Open this folder and view contentsGeneral information
Open this folder and view contentsMedication errors
Open this folder and view contentsVeterinary 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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Last updated: May 3, 2013