Medical Device Recall: CARDIOVIT AT-180. Model Number: 0A.110000; Catalog number: 3.920570
Schiller, Ag · July 24, 2024
Reason for Recall
Potential for high-frequency signal artifacts is recorded during an ECG acquisition performed by CARDIOVIT AT-180 electrocardiographs.
Distribution
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.
States Affected
IN
Quantity Affected
1084 untis
Source: FDA (openFDA Device Enforcement)
Recall number: Z-2734-2024
Status: ongoing
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