Human medicines
Acetic acid 99% - excipient
Recall
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Medicines
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08/05/2024
Recall due unknown impurity
Acetic acid 99% - excipient
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Safety information on the quality defect/recall of "Amoxilan 250 mg/5 ml - Trockensaft"
Safety warnings
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Medicines
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12/04/2024
Precautionary batch recall as a glass splinter was discovered in a 60 ml bottle.
Safety information on the quality defect/recall of "Amoxilan 250 mg/5 ml - Trockensaft"
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Amoxilan 250 mg/5 ml - Trockensaft
Recall
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Medicines
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12/04/2024
Recall due to possible contamination with glass splinters
Amoxilan 250 mg/5 ml - Trockensaft
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Tetracaine hydrochloride, active ingredient
Recall
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Medicines
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09/04/2024
Recall due to appearance of the solution
Tetracaine hydrochloride, active ingredient
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OPDIVO 10 mg/ml Konzentrat zur Herstellung einer Infusionslösung (parallel distribution Haemato Pharm GmbH)
Recall
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Medicines
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05/04/2024
Recall due to a possible incorrect closure of the crimp caps
OPDIVO 10 mg/ml Konzentrat zur Herstellung einer Infusionslösung (parallel distribution Haemato Pharm GmbH)
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OPDIVO 10 mg/ml Konzentrat zur Herstellung einer Infusionslösung (parallel distribution Orifarm GmbH)
Recall
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Medicines
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04/04/2024
Recall due to a possible incorrect closure of the crimp caps
OPDIVO 10 mg/ml Konzentrat zur Herstellung einer Infusionslösung (parallel distribution Orifarm GmbH)
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Medicinal products containing estragole
messages in brief
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15/03/2024
The committee on herbal medicinal products (HMPC) of the European Medicines Agency (EMA) published the revised Public Statement on the use of herbal medicinal products1 containing estragole.
Medicinal products containing estragole
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Amiodaron-hameln 50 mg/ml Konzentrat zur Herstellung einer lnjektions- /lnfusionslösung
Recall
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Medicines
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15/03/2024
Recall of a batch due to visible crystalline particles
Amiodaron-hameln 50 mg/ml Konzentrat zur Herstellung einer lnjektions- /lnfusionslösung
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Soolantra 10 mg/g Creme
Recall
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Medicines
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08/03/2024
Recall due to exceeding the limit value of the parameter "known impurities"
Soolantra 10 mg/g Creme
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Flux Hexal 20 mg – Kapseln and Fluoxetin 1A Pharma 20 mg – Kapseln
Recall
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Medicines
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20/02/2024
Recall due to nitrosamine contamination above the permitted daily dose
Flux Hexal 20 mg – Kapseln and Fluoxetin 1A Pharma 20 mg – Kapseln
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