ZOLL Circulation, Inc. recalls
Every recall we track for ZOLL Circulation, Inc. — 30 in all, from 2021–2025 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from ZOLL Circulation, Inc. peaked in 2021 (28); 30 since 2017.
All FDA recall records for ZOLL Circulation, Inc. since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 28 | 0 | 28 |
| 2022 | 0 | 0 | 1 | 0 | 1 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 1 | 0 | 0 | 1 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
What to do if you have a recalled ZOLL Circulation, Inc. product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All ZOLL Circulation, Inc. recalls
3 shown- Use cautionMedical device
ZOLL Circulation, Inc. recalls Brand Name: AutoPulse NXT Resuscitation System Product Name: AutoPulse NXT Platform Model/Catalog Number: Model 200
ZOLL recalls AutoPulse NXT Platform Model 200 devices that may stop chest compressions during CPR due to software error FC1060. Affected units have specific serial numbers.
ZOLLMar 4, 2025 - Lower riskMedical device
ZOLL Circulation, Inc. recalls AutoPulse Li-ion Battery used on the AutoPulse Resuscitation System Model 100. used as an adjunct to manual CPR
ZOLL Circulation, Inc. offers a range of medical devices and products for circulation monitoring and patient care.
ZOLL Circulation, Inc.Sep 22, 2022 - Lower riskMedical device
ZOLL Circulation, Inc. recalls ZOLL, REF 8700-0793-40 (SL-2593AE) SOLEX 7, Intravascular Heat Exchange Catheter Kit with central venous infusion
ZOLL recalls SOLEX 7 Intravascular Heat Exchange Catheter Kit with central venous infusion due to potential leaks from catheter or start-up kit tubing. All lots affected.
ZOLLAug 6, 2021
ZOLL Circulation, Inc. recall questions
How many recalls has ZOLL Circulation, Inc. had?
30 recalls from ZOLL Circulation, Inc. are on record with U.S. safety agencies, from 2021–2025.
What is the most recent ZOLL Circulation, Inc. recall?
ZOLL Circulation, Inc. recalls Brand Name: AutoPulse NXT Resuscitation System Product Name: AutoPulse NXT Platform Model/Catalog Number: Model 200, dated Mar 4, 2025. Every ZOLL Circulation, Inc. recall is listed on this page, newest first.
What should I do if I have a recalled ZOLL Circulation, Inc. product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new ZOLL Circulation, Inc. recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.