Recall company profile

Electro Medical Systems SA Recalls

Overview of recall records associated with Electro Medical Systems SA, including dates, categories and classifications where available.

3recall records
May 1, 2024latest record date
May 1, 2024earliest record date

Recall history in this database

Classification mix: Class II: 3.

Medical DeviceMay 1, 2024

WATER BOTTLE recall — FDA Z-1687-2024

Received complaints that bottles assembled with one batch of bottle collars can be disassembled in two parts when used under pressure (during treatment or storage if the use is not…

Class IIFDA: OngoingElectro Medical Systems SA
Medical DeviceMay 1, 2024

PIEZON Bottle recall — FDA Z-1688-2024

Received complaints that bottles assembled with one batch of bottle collars can be disassembled in two parts when used under pressure (during treatment or storage if the use is not…

Class IIFDA: OngoingElectro Medical Systems SA
Medical DeviceMay 1, 2024

CLEANER BOTTLE recall — FDA Z-1686-2024

Received complaints that bottles assembled with one batch of bottle collars can be disassembled in two parts when used under pressure (during treatment or storage if the use is not…

Class IIFDA: OngoingElectro Medical Systems SA

Understanding this recall history

This page summarizes recall records in which the official source identifies Electro Medical Systems SA as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.

Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.