PlainRecordsBrand recall history
ZOLL Circulation recalls
Every FDA recall record we found for ZOLL Circulation, newest first. Updated Oct. 11, 2026.
7
7 recalls since 2011. The most recent was on April 23, 2025.
- Last 12 months
- 0
- Most recent
- 2025-04
- Most serious (FDA Class I)
- 1
- Last 30 days
- 0
Recalls by year
2012–2026121314151617181920212223242526
Class I (FDA, most serious)Other recalls
All recalls
7- April 23, 2025Brand Name: AutoPulse NXT Resuscitation System Product Name: AutoPulse NXT Platform Model/Catalog Number… Class IAutoPulse NXT Resuscitation System may not provide adequate chest compressions or may stop compressions due to code FC1060.
- Nov. 2, 2022AutoPulse Li-ion Battery used on the AutoPulse Resuscitation System Model 100… Class IIDue to increase in Li-Ion Battery failures
- Oct. 13, 2021Zoll REF: 8700-0782-01 (IC-3893)… and 27 more products Class IILabeling update concerning potential leaks from the catheter or the start-up kit (SUK) tubing
- Dec. 3, 20147F NeuroFlo Catheter… Class IIAfter aquisition of assets of CoAxia, Zoll discovered that one lot of NeuroFlo Catheters was manufactured by another firm and an HDE supplement…
- July 30, 2014Zoll Circulation LifeBand Single Pack (accessory)… Class IIITypographical error in the Japanese legal label of the AutoPulse Resuscitation System Model 100. The label is specific to the Japanese version of the…
- Jan. 16, 2013AutoPulse Resuscitation System Model 100… Class IIComplaints associated with an unexpected stop in AutoPulse compressions.
- April 7, 2011Zoll Auto Pulse Resuscitation System… Complaints of batteries discharging prematurely and that during use the Auto Pulse Units would cease operating (providing compressions).
No recalls match.
How we match: a recall is listed here when the agency names ZOLL Circulation as the company that filed it. Sources: FDA enforcement reports and FDA-posted company announcements, CPSC recall notices and NHTSA recall campaigns.