EpiPen recall 1
Recall
|
Medicines
|
23/03/2017
The marketing authorization holder informed its supplied customers in a letter dated March 23, 2017, that there is a very low probability that the auto-injector of batch 5FA665N does not work correctly.
Worldwide, there were two customer complaints outside of Austria where the pen could not be triggered during an intended use.
Therefore, a voluntary recall of this batch is being conducted.
| Name of the medicinal product | EpiPen 300 Mikrogramm Injektionslösung in einem FertigPen |
|---|---|
| Marketing authorisation number(s) | 1-22473 |
| Marketing authorisation holder | Meda Pharma GmbH |
| Batch number(s) | 5FA665N |
| Classification of the recall | I |
| BASG reference number | INS-640.001-2044 |
Further inquiry note
Page last modified:
12/07/2022