FDAJuly 24, 2024device
CARDIOVIT AT-180. Model Number: 0A.110000; Catalog number: 3.920570
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
Potential for high-frequency signal artifacts is recorded during an ECG acquisition performed by CARDIOVIT AT-180 electrocardiographs.
What to do
FDA enforcement status: Ongoing
Brands named
schiller agschillerschiller ag
UPCs
07613365002775
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
Own something like this?
AllClear screens your whole list against every CPSC, FDA, USDA and NHTSA recall — and tells you the day a new one names something you own.
Start free — 200 items, no card →