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BEMER INT. AG Recalls

1 recall on record · February 17, 2021 to February 17, 2021 · Medical Devices

February 17, 2021Medical DevicesFDA

BEMER INT. AG recalls Bemer-Set/ Pro-Set for the following models: REF. 410201 (BEMER Pro-Set), REF. 420201 (B.BOX Professional), REF. 42010

Hazard: There potential that electromagnetic fields generated in the therapy system may cause technical defects in a patient using an insulin pumps or a malfunction of a pacemaker.

BEMER INT. AG Recalls | RecallWatchUSA