Amoxilan 250 mg/5 ml - Trockensaft

Recall | Medicines | 12/04/2024

The marketing authorisation holder informed its customers on April 12, 2024, that a glass splinter was found in a bottle of the mentioned batch. Although it is assumed to be an isolated case, it cannot be ruled out that other packs from the same batch are affected by this defect. For this reason, the batch in question is being recalled as a precautionary measure. This recall only affects the 60ml bottles.

Name of the medicinal product Amoxilan 250 mg/5 ml - Trockensaft
Marketing authorisation number(s) 1-20613
CIP code 1286346
Marketing authorisation holder G.L. Pharma GmbH
Manufacturer PenCef Pharma GmbH
Batch number(s) 23K11
Expiry date 10/31/2026
Classification of the recall1
Depth of recall Patients
BASG reference number INS-640.001-4717
Safety warnings Link Safety information on the quality defect/recall of "Amoxilan 250 mg/5 ml - Trockensaft"

Further inquiry note