Recall Atlas

ZOLL Circulation recalls

3 official recalls and safety alerts involving ZOLL Circulation since 2021-10, from FDA · Device. Newest first. Check the official notice for exact models and batch codes.

This list only includes recalls Recall Atlas has collected since 2021-10. A product not listed here may still be affected; check with ZOLL Circulation or the relevant agency.

  1. 2025-04-23
  2. US
    Drugs & medicalClass I

    ZOLL Circulation, Inc. recalls Brand Name: AutoPulse NXT Resuscitation System Product Name: AutoPulse NXT Platform Model/Catalog Number: Model 200 (Catalog Number:…

    AutoPulse NXT Resuscitation System may not provide adequate chest compressions or may stop compressions due to code FC1060.

    FDA · DeviceZOLL Circulation, Inc.US: AL, CA, CT, FL, IL, KS, LA, MN, MO, MT, NC, ND, NM, NY, OH, OK< PA, TX, WI…Official notice →
  3. 2022-11-02
  4. US
    Drugs & medicalClass II

    ZOLL Circulation, Inc. recalls AutoPulse Li-ion Battery used on the AutoPulse Resuscitation System Model 100. used as an adjunct to manual CPR

    Due to increase in Li-Ion Battery failures

    FDA · DeviceZOLL Circulation, Inc.U.S.: AK, AL, AR, AZ, CA, CO, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA,…Official notice →
  5. 2021-10-13
  6. US
    Drugs & medicalClass II

    ZOLL Circulation, Inc. recalls ZOLL, REF 8700-0793-40 (SL-2593AE) SOLEX 7, Intravascular Heat Exchange Catheter Kit with central venous infusion capabilities (3 lumens),…

    Labeling update concerning potential leaks from the catheter or the start-up kit (SUK) tubing

    FDA · DeviceZOLL Circulation, Inc.Worldwide distribution - US Nationwide distribution in the states of AL, AZ,…Official notice →