Fludeoxyglucose
Recall
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Medicines
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24/11/2017
The distribution partner for the marketing authorization holder, "DSD Pharma GmbH", informed its supplied customers in a letter dated November 15, 2017, that the qualified person for batch 171115FDG01 has not issued a batch release and that the batch in question may therefore not be used.
Name of the medicinal product | [18F]Fludeoxyglucose Biont 200-2200 MBq/ml Injektionslösung |
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Marketing authorisation number(s) | 4-00048 |
Marketing authorisation holder | Biont a.s. Vertrieb und Durchführung Rückruf: DSD Pharma GmbH |
Batch number(s) | 171115FDG01 |
Classification of the recall | 3 |
BASG reference number | INS-640.001-2346 |
Further inquiry note
Page last modified:
12/07/2022