CARDIOVIT AT-180. Model Number: 0A.110000; Catalog number... (Schiller, Ag Altgasse 68 Baar Switzerland) – potential for high-frequency signal a... (2024)
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
CARDIOVIT AT-180. Model Number: 0A.110000; Catalog number: 3.920570
Brand
Schiller, Ag Altgasse 68 Baar Switzerland
Lot Codes / Batch Numbers
UDI-DI: 07613365002775. All serial numbers, all software versions.
Products Sold
UDI-DI: 07613365002775. All serial numbers, all software versions.
Schiller, Ag Altgasse 68 Baar Switzerland is recalling CARDIOVIT AT-180. Model Number: 0A.110000; Catalog number: 3.920570 due to Potential for high-frequency signal artifacts is recorded during an ECG acquisition performed by CARDIOVIT AT-180 electrocardiographs.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Potential for high-frequency signal artifacts is recorded during an ECG acquisition performed by CARDIOVIT AT-180 electrocardiographs.
Recommended Action
Per FDA guidance
Single US consignee was notified via letter on 07/24/2024. The consignee was instructed to send the notification to all consignees if further distributed, respond to the notification and return the reply form, and updated the affected devices according to Service Instructions. At the user level, customer are requested to respond by sending the Customer Reply Form back to their authorized distributor as confirmation that the Field Safety Notice was read and understood.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
FL, IN
Page updated: Jan 10, 2026