FDA Device Intelligence
Home › Zoll Circulation, Inc. › RTX CIRCULATING CASSETTE WITHOUT ELECTROLYTE

RTX CIRCULATING CASSETTE WITHOUT ELECTROLYTE

Zoll Circulation, Inc. · Model NA · UDI-DI 00849111075459

NCX Prescription
10
510(k) clearances
4,407
Adverse events (44 deaths)
35
Recalls
4
Facilities

Description

The InnerCool RTx Circulating Cassette is part of the InnerCool RTx Endovascular Cooling System. It cools the heat-transfer fluid that circulates through the Cassette and Catheters.

Recalls

DateFirmReason
2021-08-06ZOLL Circulation, Inc.Labeling update concerning potential leaks from the catheter or the start-up kit (SUK) tubing
2021-08-06ZOLL Circulation, Inc.Labeling update concerning potential leaks from the catheter or the start-up kit (SUK) tubing
2021-08-06ZOLL Circulation, Inc.Labeling update concerning potential leaks from the catheter or the start-up kit (SUK) tubing
2021-08-06ZOLL Circulation, Inc.Labeling update concerning potential leaks from the catheter or the start-up kit (SUK) tubing
2021-08-06ZOLL Circulation, Inc.Labeling update concerning potential leaks from the catheter or the start-up kit (SUK) tubing
2021-08-06ZOLL Circulation, Inc.Labeling update concerning potential leaks from the catheter or the start-up kit (SUK) tubing
2021-08-06ZOLL Circulation, Inc.Labeling update concerning potential leaks from the catheter or the start-up kit (SUK) tubing
2021-08-06ZOLL Circulation, Inc.Labeling update concerning potential leaks from the catheter or the start-up kit (SUK) tubing
2021-08-06ZOLL Circulation, Inc.Labeling update concerning potential leaks from the catheter or the start-up kit (SUK) tubing
2021-08-06ZOLL 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 docs
Data 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.