Safety information on the medical device Disinfection system with 3% peroxide New
Safety warnings
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Medical devices
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09/07/2025
The Federal Office for Safety in Health Care (BASG) warns against the disinfection system with 3% peroxide from the manufacturer DISOP S.A. Only certain batch numbers are affected.
According to previous investigations by DISOP S.A., it is possible that some neutralisation tablets used together with the solution do not dissolve in time and therefore do not completely neutralise the peroxide mixture.
The following batch numbers are affected: FSN_2025_1_ANNEX 1_EN_v2.pdf
According to current estimates, around 1340 units of the above products are affected in Austria.
The BASG has received 0 reports of incidents from Austria so far.
| Medical devices | Disinfection system with 3% peroxide |
|---|---|
| Manufacturer | DISOP S.A. |
| Batch number(s) | FSN_2025_1_ANHANG 1_DE_v2.pdf |
| Corrective actions | The BASG recommends verifying the batch numbers of the disinfection system containing 3% hydrogen peroxide to ensure safety. If a product is affected, please discontinue its use immediately. The product can be returned to your optician, specialist retailer, or point of purchase. |
| Further information Link | FSN_2025_1_ANHANG 1_DE_v2.pdf |
| Company letter (pdf) Link | FSN_2025_01_Verbraucher_DE_v2_13-06-2025.docx |
Further inquiry note
Page last modified:
09/07/2025