Sprycel 100 mg Filmtabletten
Recall
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Medicines
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15/02/2019
The parallel distributor „HAEMATO PHARM GmbH“ informed its customers on February 14, 2019 that the supply chain is not fully documented and GDP-guidelines are not met. Therefore all parallel distributed batches referring to EAN-Code 90888842026989 are recalled as a precautionary measure in Austria.
| Name of the medicinal product | SPRYCEL 100 mg Filmtabletten |
|---|---|
| Marketing authorisation number(s) | EU/1/06/363/010-011 (EAN-Code 90888842026989) |
| Marketing authorisation holder | Bristol-Myers Squibb Pharma EEIG Paralleldistribution: HAEMATO PHARM GmbH |
| Batch number(s) | AAU8209, AAX0992, AAY1632 |
| Classification of the recall | 1 |
| BASG reference number | INS-640.001-2776 |
Further inquiry note
Page last modified:
08/11/2019