https://plainrecords.com/brand/zoll-circulation/New recalls of ZOLL Circulation from FDA, CPSC and NHTSA records.en-ushttps://plainrecords.com/recall/device/z-1533-2025/https://plainrecords.com/recall/device/z-1533-2025/Wed, 23 Apr 2025 00:00:00 +0000AutoPulse NXT Resuscitation System may not provide adequate chest compressions or may stop compressions due to code FC1060.https://plainrecords.com/recall/device/z-0118-2023/https://plainrecords.com/recall/device/z-0118-2023/Wed, 02 Nov 2022 00:00:00 +0000Due to increase in Li-Ion Battery failureshttps://plainrecords.com/recall/device/z-0039-2022/https://plainrecords.com/recall/device/z-0039-2022/Wed, 13 Oct 2021 00:00:00 +0000Labeling update concerning potential leaks from the catheter or the start-up kit (SUK) tubinghttps://plainrecords.com/recall/device/z-0477-2015/https://plainrecords.com/recall/device/z-0477-2015/Wed, 03 Dec 2014 00:00:00 +0000After 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 the product was not filed.https://plainrecords.com/recall/device/z-2090-2014/https://plainrecords.com/recall/device/z-2090-2014/Wed, 30 Jul 2014 00:00:00 +0000Typographical error in the Japanese legal label of the AutoPulse Resuscitation System Model 100. The label is specific to the Japanese version of the product.https://plainrecords.com/recall/device/z-0658-2013/https://plainrecords.com/recall/device/z-0658-2013/Wed, 16 Jan 2013 00:00:00 +0000Complaints associated with an unexpected stop in AutoPulse compressions.https://plainrecords.com/recall/device/z-1904-2011/https://plainrecords.com/recall/device/z-1904-2011/Thu, 07 Apr 2011 00:00:00 +0000Complaints of batteries discharging prematurely and that during use the Auto Pulse Units would cease operating (providing compressions).