Schiller, Ag: Medical Device Recall in 2024 - (Recall #: Z-2734-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

CARDIOVIT AT-180. Model Number: 0A.110000; Catalog number: 3.920570

Product Classification:

Class II

Date Initiated: July 24, 2024

Date Posted: September 4, 2024

Recall Number: Z-2734-2024

Event ID: 95074

Reason for Recall:

Potential for high-frequency signal artifacts is recorded during an ECG acquisition performed by CARDIOVIT AT-180 electrocardiographs.

Status: Ongoing

Product Quantity: 1084 untis

Code Information:

UDI-DI: 07613365002775. All serial numbers, all software versions.

Distribution Pattern:

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.

Voluntary or Mandated:

Voluntary: Firm initiated