Human medicines

Recall "Melphalan Koanaa 50 mg i.v. Powder and solvent for solution for injection or solution for infusion" (active ingredient melphalan)

Safety warnings | Medicines | 11/08/2017
The drug "Melphalan Koanaa 50 mg i.v. Powder and Solvent for Solution for Injection or Solution for Infusion" is being recalled due to suspected drug counterfeiting.
Recall "Melphalan Koanaa 50 mg i.v. Powder and solvent for solution for injection or solution for infusion" (active ingredient melphalan) Read more

Vibravenös

Recall | Medicines | 11/08/2017

The marketing authorization holder has informed its supplied customers in a letter dated August 10, 2017, that a batch of Vibravenous - Ampoules with…

Vibravenös Read more

Melphalan

Recall | Medicines | 11/08/2017

"Koanaa Healthcare GmbH" has informed its customers in a letter dated August 10, 2017, that the further marketing of "Melphalan Koanaa 50 mg i.v.…

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Quassia Similiaplex

Recall | Medicines | 27/07/2017

"Pascoe Pharm. Präparate GmbH" as the holder of the registration as a homeopathic medicinal speciality of "Quassia Similiaplex drops" has informed its…

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Edronax

Recall | Medicines | 27/07/2017

The marketing authorization holder has informed its supplied customers in a letter dated July 25, 2017, that a test result within the scope of a…

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Buerlecithin

Recall | Medicines | 05/07/2017

The marketing authorization holder has informed its supplied customers in a letter dated July 04, 2017, that individual bottles filled with distilled…

Buerlecithin Read more

Mucosolvan Lutschpastillen

Recall | Medicines | 26/06/2017

The marketing authorization holder has informed its supplied customers in a letter dated June 21, 2017, that in the course of stability tests a trend…

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Trobalt

Recall | Medicines | 26/06/2017

The marketing authorization holder has informed its supplied customers in a letter dated 23.06.2017 that due to the global decision of the company,…

Trobalt Read more

Elotrace

Recall | Medicines | 24/05/2017

The marketing authorization holder has informed its supplied customers in a letter dated May 23, 2017, that increased black visible particles have…

Elotrace Read more

Albiomin

Recall | Medicines | 28/04/2017

The marketing authorization holder has informed its supplied customers in a letter dated April 27, 2017, that the affected batches are being recalled…

Albiomin Read more
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