Home › Zoll Circulation, Inc. › InnerCool RTx 10.7F Standard Catheter
InnerCool RTx 10.7F Standard Catheter
Zoll Circulation, Inc. · Model NA · UDI-DI 00849111075381
NCX
Prescription
1
510(k) clearances
4,436
Adverse events (44 deaths)
35
Recalls
4
Facilities
Description
An endovascular catheter having a heat exchange element at the distal end, through which a thermal transfer fluid is circulated to cool or warm the blood, and which has 10.7 Fr diameter.
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2021-08-06 | ZOLL Circulation, Inc. | Labeling update concerning potential leaks from the catheter or the start-up kit (SUK) tubing |
| 2021-08-06 | ZOLL Circulation, Inc. | Labeling update concerning potential leaks from the catheter or the start-up kit (SUK) tubing |
| 2021-08-06 | ZOLL Circulation, Inc. | Labeling update concerning potential leaks from the catheter or the start-up kit (SUK) tubing |
| 2021-08-06 | ZOLL Circulation, Inc. | Labeling update concerning potential leaks from the catheter or the start-up kit (SUK) tubing |
| 2021-08-06 | ZOLL Circulation, Inc. | Labeling update concerning potential leaks from the catheter or the start-up kit (SUK) tubing |
| 2021-08-06 | ZOLL Circulation, Inc. | Labeling update concerning potential leaks from the catheter or the start-up kit (SUK) tubing |
| 2021-08-06 | ZOLL Circulation, Inc. | Labeling update concerning potential leaks from the catheter or the start-up kit (SUK) tubing |
| 2021-08-06 | ZOLL Circulation, Inc. | Labeling update concerning potential leaks from the catheter or the start-up kit (SUK) tubing |
| 2021-08-06 | ZOLL Circulation, Inc. | Labeling update concerning potential leaks from the catheter or the start-up kit (SUK) tubing |
| 2021-08-06 | ZOLL Circulation, Inc. | Labeling update concerning potential leaks from the catheter or the start-up kit (SUK) tubing |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
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.
