Official announcements
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Recall
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Medicines
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24/10/2016
The marketing authorization holder informed its supplied customers in a letter dated October 12, 2016, that an impurity, "lmpurity D", was detected in the course of stability tests, which in the measured concentration does not indicate any health…
Recall
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Medicines
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24/10/2016
The marketing authorization holder informed its supplied customers in a letter dated October 13, 2016, that an impurity, "lmpurity D", was detected during stability tests. In the measured concentration there is no health risk for the patients. A…
Recall
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Medicines
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18/10/2016
Gedeon Richter Plc has informed their supplied customers by letter dated 12/10/2016 that above mentioned batches of "Lisvy 60 microgram/24 hours + 13 microgram/24 hours Transdermal Patch" are recalled. Stability data for these batches indicated a…
Recall
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Medicines
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14/10/2016
CSL Behring as distributor of the product Helixate NexGen has, in coordination with the marketing authorization holder Bayer Pharma AG, informed its supplied customers in a letter dated October 11, 2016, that the above mentioned batches of Helixate…
Recall
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Medicines
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19/09/2016
In a letter dated 19.09.2016, the marketing authorization holder informed its customers that yellow-brownish particles had been detected in the above batch and that a recall was therefore being carried out. The particles are traces of corrosion…
Recall
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Medicines
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16/09/2016
The marketing authorization holder informed its supplied customers in a letter dated 13.09.2016 that its batch of "Chlorhexidine digluconate Sage 20 mg/ml impregnated wipe" must be recalled as it is possibly microbiologically contaminated withbecause…
Safety warnings
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Medicines
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06/09/2016
Novo Nordisk is recalling 55 lots of GlucaGen HypoKit worldwide because in some cases the needle has come loose from the pre-filled syringe. In Austria, one batch is affected.
Recall
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Medicines
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06/09/2016
The marketing authorization holder has informed its customers as well as pharmacies, institutional pharmacies, physicians in private practice and patient organizations by letter dated 06.09.2016 that there is a possibility of a detached needle from…
Recall
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Medicines
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17/08/2016
The marketing authorization holder has informed its supplied customers in a letter dated August 2, 2016, that the above-mentioned batches of "Amiodarone 150 mg i.v. Carino" are being recalled. During a routine check of reserve samples,…
Recall
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Medicines
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11/08/2016
The marketing authorization holder informed its supplied customers in a letter dated August 10, 2016, that the above-mentioned batches of Kogenate®Bayer are being recalled. Stability data for these batches indicated a faster than usual decline in…