Medical DeviceApr 23, 2025
AutoPulse NXT Platform recall — FDA Z-1533-2025
AutoPulse NXT Resuscitation System may not provide adequate chest compressions or may stop compressions due to code FC1060.
Class IFDA: OngoingZOLL Circulation, Inc.
Recall history in this database
Classification mix: Class II: 29, Class I: 1.
Medical DeviceNov 2, 2022
ZOLL Circulation AutoPulse Li-ion Battery used on the AutoPulse Resuscitation System Model recall — FDA Z-0118-2023
Due to increase in Li-Ion Battery failures
Class IIFDA: OngoingZOLL Circulation, Inc.
Medical DeviceOct 13, 2021
ZOLL Circulation ZOLL, REF 8700-0793-40 (SL-2593AE) SOLEX 7, Intravascular Heat Exchange recall — FDA Z-0043-2022
Labeling update concerning potential leaks from the catheter or the start-up kit (SUK) tubing
Class IIFDA: TerminatedZOLL Circulation, Inc.
Medical DeviceOct 13, 2021
ZOLL Circulation ZOLL, REF 8700-0787-40 (IC-3893AE), ICY Intravascular Heat Exchange recall — FDA Z-0046-2022
Labeling update concerning potential leaks from the catheter or the start-up kit (SUK) tubing
Class IIFDA: TerminatedZOLL Circulation, Inc.
Medical DeviceOct 13, 2021
ZOLL Circulation Zoll, REF 8700-0657-40 (IC-3893AE), ICY Intravascular Heat Intravascular recall — FDA Z-0057-2022
Labeling update concerning potential leaks from the catheter or the start-up kit (SUK) tubing
Class IIFDA: TerminatedZOLL Circulation, Inc.
Medical DeviceOct 13, 2021
ZOLL Circulation Zoll, REF 8700-0695-40 (IC-3893AE), ICY Intravascular Heat Intravascular recall — FDA Z-0056-2022
Labeling update concerning potential leaks from the catheter or the start-up kit (SUK) tubing
Class IIFDA: TerminatedZOLL Circulation, Inc.
Medical DeviceOct 13, 2021
Zoll REF: 8700-0793-14 (SL-2593CO), SOLEX 7 Intravascular Heat Exchange Catheter Kit with recall — FDA Z-0052-2022
Labeling update concerning potential leaks from the catheter or the start-up kit (SUK) tubing
Class IIFDA: TerminatedZOLL Circulation, Inc.
Medical DeviceOct 13, 2021
ZOLL Circulation ZOLL, REF 8700-0781-40 (CL-2295AE), COOL LINE Intravascular Heat Exchange recall — FDA Z-0045-2022
Labeling update concerning potential leaks from the catheter or the start-up kit (SUK) tubing
Class IIFDA: TerminatedZOLL Circulation, Inc.
Medical DeviceOct 13, 2021
ZOLL Circulation Zoll, REF 8700-000871-40, Quattro (Heparin) IVTM Disposable Pack and Start recall — FDA Z-0065-2022
Labeling update concerning potential leaks from the catheter or the start-up kit (SUK) tubing
Class IIFDA: TerminatedZOLL Circulation, Inc.
Medical DeviceOct 13, 2021
ZOLL Circulation Zoll, REF 8700-000866-01, ICY IVTM Disposable Pack and Start UP Kit (6 ft.) recall — FDA Z-0060-2022
Labeling update concerning potential leaks from the catheter or the start-up kit (SUK) tubing
Class IIFDA: TerminatedZOLL Circulation, Inc.
Medical DeviceOct 13, 2021
ZOLL Circulation Zoll, REF: 8700-0791-01 (IC-4593), Premium Access Kit QUATTRO recall — FDA Z-0040-2022
Labeling update concerning potential leaks from the catheter or the start-up kit (SUK) tubing
Class IIFDA: TerminatedZOLL Circulation, Inc.
Medical DeviceOct 13, 2021
ZOLL Circulation Zoll, REF 8700-0781-03 (CL-2295AE), COOLINE Intravascular Heat recall — FDA Z-0054-2022
Labeling update concerning potential leaks from the catheter or the start-up kit (SUK) tubing
Class IIFDA: TerminatedZOLL Circulation, Inc.
Medical DeviceOct 13, 2021
Zoll REF: 8700-0782-14 (IC-3893CO), ICY Intravascular Heat Exchange Catheter Kit with recall — FDA Z-0050-2022
Labeling update concerning potential leaks from the catheter or the start-up kit (SUK) tubing
Class IIFDA: TerminatedZOLL Circulation, Inc.
Medical DeviceOct 13, 2021
ZOLL Circulation Zoll, REF 8700-000870-40, ICY (Heparin) IVTM Disposable Pack and Start UP recall — FDA Z-0064-2022
Labeling update concerning potential leaks from the catheter or the start-up kit (SUK) tubing
Class IIFDA: TerminatedZOLL Circulation, Inc.
Medical DeviceOct 13, 2021
ZOLL Circulation Zoll, REF 8700-000865-01, Cool Line IVTM Disposable Pack and Start UP Kit recall — FDA Z-0059-2022
Labeling update concerning potential leaks from the catheter or the start-up kit (SUK) tubing
Class IIFDA: TerminatedZOLL Circulation, Inc.
Medical DeviceOct 13, 2021
ZOLL Circulation Zoll, REF: 8700-0783-03 (IC-4593AE) QUATTRO Intravascular Heat Exchange recall — FDA Z-0053-2022
Labeling update concerning potential leaks from the catheter or the start-up kit (SUK) tubing
Class IIFDA: TerminatedZOLL Circulation, Inc.
Medical DeviceOct 13, 2021
ZOLL Circulation Zoll, REF 8700-000867-01, Quattro IVTM Disposable Pack and Start UP Kit recall — FDA Z-0061-2022
Labeling update concerning potential leaks from the catheter or the start-up kit (SUK) tubing
Class IIFDA: TerminatedZOLL Circulation, Inc.
Medical DeviceOct 13, 2021
ZOLL Circulation ZOLL, REF 8700-0793-01 (SL-2593) Premium Access Kit SOLEX 7, Intravascular recall — FDA Z-0042-2022
Labeling update concerning potential leaks from the catheter or the start-up kit (SUK) tubing
Class IIFDA: TerminatedZOLL Circulation, Inc.
Medical DeviceOct 13, 2021
ZOLL Circulation ZOLL, REF: 8700-0781-01 (CL-2295), COOL LINE, Intravascular Heat Exchange recall — FDA Z-0041-2022
Labeling update concerning potential leaks from the catheter or the start-up kit (SUK) tubing
Class IIFDA: TerminatedZOLL Circulation, Inc.
Medical DeviceOct 13, 2021
ZOLL Circulation ZOLL, REF 8700-0781-14 (CL-2295CO), COOL LINE Intravascular Heat Exchange recall — FDA Z-0044-2022
Labeling update concerning potential leaks from the catheter or the start-up kit (SUK) tubing
Class IIFDA: TerminatedZOLL Circulation, Inc.
Medical DeviceOct 13, 2021
Zoll REF: 8700-0782-40 (IC-3893AE), ICY Intravascular Heat Exchange Catheter Kit with recall — FDA Z-0047-2022
Labeling update concerning potential leaks from the catheter or the start-up kit (SUK) tubing
Class IIFDA: TerminatedZOLL Circulation, Inc.
Medical DeviceOct 13, 2021
ZOLL Circulation Zoll, REF 8700-000868-01, Solex 7 IVTM Disposable Pack and Start UP Kit recall — FDA Z-0062-2022
Labeling update concerning potential leaks from the catheter or the start-up kit (SUK) tubing
Class IIFDA: TerminatedZOLL Circulation, Inc.
Medical DeviceOct 13, 2021
ZOLL Circulation Zoll, REF 8700-000872-40, SOLEX 7(Heparin) IVTM Disposable Pack and Start recall — FDA Z-0066-2022
Labeling update concerning potential leaks from the catheter or the start-up kit (SUK) tubing
Class IIFDA: TerminatedZOLL Circulation, Inc.
Medical DeviceOct 13, 2021
ZOLL Circulation Zoll, REF 8700-000766-01, Quattro IVTM Premium Disposable Pack and Start UP recall — FDA Z-0058-2022
Labeling update concerning potential leaks from the catheter or the start-up kit (SUK) tubing
Class IIFDA: TerminatedZOLL Circulation, Inc.
Understanding this recall history
This page summarizes recall records in which the official source identifies ZOLL Circulation, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.