ZOLL Circulation, Inc. recalls
6 recalls in our records from 2013 to 2025: 6 FDA medical devices.
Recalls with full detail pages
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ZOLL Circulation, Inc. medical device recall: Brand Name: AutoPulse NXT Resuscitation System Product Name:…
AutoPulse NXT Resuscitation System may not provide adequate chest compressions or may stop compressions due to code FC1060.
Earlier and other recalls
These link to the official agency notice.
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ZOLL Circulation, Inc. medical device recall: AutoPulse Li-ion Battery used on the AutoPulse Resuscitation System… Official notice ↗
Due to increase in Li-Ion Battery failures
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ZOLL Circulation, Inc. medical device recall: Zoll REF: 8700-0782-01 Official notice ↗
Labeling update concerning potential leaks from the catheter or the start-up kit (SUK) tubing
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ZOLL Circulation, Inc. medical device recall: 7F NeuroFlo Catheter Official notice ↗
After aquisition of assets of CoAxia, Zoll discovered that one lot of NeuroFlo Catheters was manufactured by another firm and an HDE supplement listing as the owner of…
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Zoll Circulation, Inc. medical device recall: Zoll Circulation LifeBand Single Pack Official notice ↗
Typographical error in the Japanese legal label of the AutoPulse Resuscitation System Model 100. The label is specific to the Japanese version of the product.
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Zoll Circulation, Inc. medical device recall: AutoPulse Resuscitation System Model 100 Official notice ↗
Complaints associated with an unexpected stop in AutoPulse compressions.
Firm names are matched across agencies by name only. Different companies with similar names may be grouped together; check each official notice.