Amoxilan 500mg/5ml - Trockensaft
Recall
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Medicines
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06/03/2025
The marketing authorisation holder informed its customers on March 05, 2025, that it cannot be ruled out that there may be glass splinters in the bottles of batch 24L19 “Amoxilan 500 mg/5 ml - Trockensaft”. For this reason, the mentioned batch is being recalled as a precautionary measure. This recall only affects the 60ml bottles.
Name of the medicinal product | Amoxilan 500mg/5ml - Trockensaft |
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Marketing authorisation number(s) | 1-20614 |
CIP code | 1286369 |
Marketing authorisation holder | G.L. Pharma GmbH |
Manufacturer | PenCef Pharma |
Batch number(s) | 24L19 |
Expiry date | 03/31/2027 |
Classification of the recall | 1 |
Depth of recall | Patients |
BASG reference number | INS-640.001-5099 |
Safety warnings Link | Safety information on the quality defect/recall of "Amoxilan 500 mg/5 ml – Trockensaft" |
Further inquiry note
Page last modified:
05/03/2025