Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
CARDIOVIT AT-180. Model Number: 0A.110000 Recalled by Schiller, Ag Due to Potential for high-frequency signal artifacts is recorded during...
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 Schiller, Ag directly.
Affected Products
CARDIOVIT AT-180. Model Number: 0A.110000; Catalog number: 3.920570
Quantity: 1084 untis
Why Was This Recalled?
Potential for high-frequency signal artifacts is recorded during an ECG acquisition performed by CARDIOVIT AT-180 electrocardiographs.
Where Was This Sold?
Worldwide - US distribution in the state of Florida and the countries of Austria, Belgium, Switzerland, Cyprus, Czechia, Germany, Spain, Finland, France, Great Britain, Ireland, Iceland, Italy, Luxembourg, Malta, The Netherlands, Norway, Portugal, Romania, Sweden, Slovenia, Australia, The United Arab Emirates, Bahrain, Canada, China, Israel, India, Jordan, Kuwait, Libya, Morocco, Malaysia, Qatar, Serbia, South Africa.
About Schiller, Ag
Schiller, Ag has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report