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uCor Heart Failure and Arrhythmia Management System
ZOLL MANUFACTURING CORPORATION · Model Sensor · UDI-DI 00855778005302
1
510(k) clearances
6
Adverse events
2
Recalls
68
Facilities
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2022-09-02 | Baxter Healthcare Corporation | Labeling has incorrect or incomplete Unique Device Identification (UDI) information; and the barcodes are not compliant with GS-1 standards. |
| 2015-12-01 | Partners In Medicine Llc | Device non-conformity which may lead to an incorrect oscillometric measurement of upper arm blood pressure values in some subjects - mainly in tall and slim persons (overestimation |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.