Official announcements
Recall
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Medicines
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20/06/2013
The marketing authorization holder has informed its supplied customers in a letter dated June 19, 2013, that due to a manufacturing problem and the associated risk of microbial contamination with "Sphingomonas yanoikuyae", the above mentioned batches…
Replacement
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Medicines
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19/06/2013
The marketing authorization holder informed its supplied customers in a letter dated June 18, 2013, that due to an individual complaint from the German market regarding a plastic ampoule leaking at the neck of the bottle, batch 12FHL21 will be…
Replacement
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Veterinary Medicines
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05/06/2013
The marketing authorization holder informed its supplied customers in a letter dated June 4, 2013, that individual bottles of the batch 1112208AE of the product Vitasol AD3EC Injection Solution for Animals, package size 5 x 100 ml, had been placed on…
Recall
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Medicines
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04/06/2013
The marketing authorization holder informed its supplied customers in a letter dated June 3, 2013, that in the course of stability tests after 24 months of storage, non-specification-compliant results were found for a batch of Cileste in the…
Recall
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Medicines
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24/05/2013
The marketing authorization holder has informed its supplied customers in a letter dated 24.05.2013 that particles were observed in some vials. For this reason, the above mentioned batches are recalled as a precautionary measure.
Recall
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Medicines
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23/05/2013
During a routine test, leaks in the area of the predetermined breaking point at the neck of an amber glass ampoule of the size 1 ml were discovered in a product batch that has not yet been released, which are due to a material defect in the glass.…
Safety warnings
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messages in brief
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18/04/2013
Methotrexate (various preparations)
messages in brief
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18/04/2013
As of 01.07.2013, the transmission of Austrian product information texts is to take place via the eService "Marketing Authorization and Lifecycle Drug Specialties ". The e-mail address spc@ages.at will no longer be available as of 31.01.2014. With…
Recall
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Medicines
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18/04/2013
The marketing authorization holder informed its customers in a letter dated April 18, 2013, that due to a technical defect during production, isolated particles were observed in the prefilled syringes. In the course of a 100% inspection, prefilled…
Recall
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Medicines
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19/03/2013
The marketing authorization holder has informed its supplied customers and medical home pharmacies that a microbiological contamination has been detected in a batch of the drug "Magnesium Verla i.v./i.m. Injection Solution" from Verla-Pharm…
