On July 23, 2025, Zeytun Pharmaceuticals LLC submitted a request to the Analytical Expertise Center under the Ministry of Health for the voluntary recall of two medicinal products. The details are as follows:
- Paracetamol – 125 mg/supp., trade name “Para-Denk 125 Suppos”, rectal suppositories, pack of 10 (2×5) in blisters, in a cardboard box. The marketing authorization holder is Denk Pharma GmbH Ko.KG / Germany. The damaged batches are:
- Batch No. 27339, expiry date: 31.03.2026
- Batch No. 27839, expiry date: 01.08.2026
- Batch No. 26906, expiry date: 31.07.2025
- Paracetamol – 250 mg/supp., trade name “Para-Denk 250 Suppos”, rectal suppositories, pack of 10 (2×5) in blisters, in a cardboard box. The marketing authorization holder is Denk Pharma GmbH Ko.KG / Germany. The damaged batches are:
- Batch No. 27292, expiry date: 28.02.2026
- Batch No. 27822, expiry date: 30.06.2026
The reason for the recall is packaging defects (leakages).
The recall classification has been determined as Class 3 (where the defect is unlikely to cause harm to a person’s health),
and the recall level as Level C (up to the wholesale distributor level).
The stated defects were confirmed during inspection in both products.
In accordance with the “Rules for the Recall of Medicinal Products,” approved by the Decision No. 460 of the Cabinet of Ministers of the Republic of Azerbaijan dated November 27, 2019, a decision has been made to recall the above-mentioned medicinal products.
