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Schiller, Ag recalls CARDIOVIT AT-180. Model Number: 0A.110000; Catalog number: 3.920570
Recalled September 4, 2024 · FDA recall Z-2734-2024 · Schiller, Ag
Hazard
Potential for high-frequency signal artifacts is recorded during an ECG acquisition performed by CARDIOVIT AT-180 electrocardiographs. · FDA Class II
Units
1084 untis
Sold at
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.
Description
Potential for high-frequency signal artifacts is recorded during an ECG acquisition performed by CARDIOVIT AT-180 electrocardiographs.
Product
CARDIOVIT AT-180. Model Number: 0A.110000; Catalog number: 3.920570
Manufacturer(s)
Schiller, Ag
Made in
Switzerland
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →