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.

Recall due to microbial contamination.

Recall due to a deviation during filling.

Recall due to potential microbiological contamination.

Precautionary recall because the efficacy may be reduced.

Recall of one batch of Adolorin Ibuforte 400 mg Dragees due to reduced release of the active substance.