Recall due to azido contamination above the acceptable limit.

Recall of two batches due to an incorrect expiry date

One affected batch contains too few needles

Incorrect package leaflet was enclosed with one batch

Recall of several batches due to dosing problems

Recall of one batch due to a deviation during stability monitoring analysis.

Recall due to a possible exceedance of the permitted exposure levels for a derivative of the active substance.

Decrease in plasma donations with simultaneous increase in demand for immunoglobulins.

Recall of one affected batch of Vistabel because there is a risk of incorrect dilution and administration of double dose.

Recall due to a slight excess of microbial purity.