The Federal Office for Safety in Health Care (BASG) warns of a counterfeit medical device that could be mistaken for the legitimate product "Needleless Airtight Infusion Connector Protector" from the manufacturer "Zhejiang Runqiang Medical Instruments Co., Ltd.".

Recall due to the possibility of powder clumping in the capsule

The Federal Office for Safety in Health Care (BASG) warns of a counterfeit medical device that could be mistaken for the legitimate product "Sculptra" from the manufacturer "Q-Med AB".

Recall due to incorrect labelling of active substance content

Recall due to impurities and low viscosity

The Federal Office for Safety in Health Care (BASG) warns of non-conforming subcutaneous and absorbable PDO threads, marketed as “ARIEL PDO Threads”, along with associated cannulas intended for mechanical tightening of loose and sagging skin (facelifting).

Recall due to contamination with petroleum jelly

Recall due to deviations from quality standards at the active ingredient manufacturer

The BASG has announced that the first four modules of the European Database on Medical Devices (EUDAMED) will be mandatory to use as from 28 May 2026.

Recall due to reduced release of active pharmaceutical ingredient