Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Bemer-Set/ Pro-Set for the following models: REF. 410201 (BEMER Pro-Set) Recalled by BEMER INT. AG Due to There potential that electromagnetic fields generated in the...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact BEMER INT. AG directly.
Affected Products
Bemer-Set/ Pro-Set for the following models: REF. 410201 (BEMER Pro-Set), REF. 420201 (B.BOX Professional), REF. 420100 (B.BOX CLASSIC), REF. 410100 (BEMER Classic-Set), REF. 420200 (B.BOX Professional), and REF. 410200 (BEMER Pro - Set)
Quantity: 197,724 units
Why Was This Recalled?
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.
Where Was This Sold?
US
About BEMER INT. AG
BEMER INT. AG has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report