ZOLL Circulation recalls

ZOLL Circulation has 33 recalls on record with the FDA and USDA, the earliest in 2013 and the latest reported on 23 Apr 2025. 2 are still ongoing. The most frequent reason is sterility.

Total recalls33since 2013

Last 12 months0reported

Class I13% of total

Ongoing2latest 23 Apr 2025

Recalls per month, last 24 months

click a bar for that month

0Oct '24 0 0 0Jan '25 0 0 1Apr 0 0 0Jul 0 0 0Oct 0 0 0Jan '26 0 0 0Apr 0 0 0Jul 0 0

Severity split

Class I 1 3%Class II 31 94%Class III 1 3%

Why zoll circulation is recalled

Product types

By year

202513%
202213%
20212885%
201426%
201313%

Ongoing zoll circulation recalls

2 active

Reported	Class	Recall	Company	Reason	Where
23 Apr 2025Device	CLASS I	AutoPulse NXT Resuscitation System AutoPulse NXT Platform recalled	ZOLL Circulation	Device Malfunction	18 states
2 Nov 2022Device	CLASS II	AutoPulse Li-ion Battery used on the AutoPulse Resuscitation System recalled	ZOLL Circulation	Device Malfunction	47 states

All zoll circulation recalls, newest first

33 total

Reported	Class	Recall	Company	Reason	Where
23 Apr 2025Device	CLASS I	AutoPulse NXT Resuscitation System AutoPulse NXT Platform recalled	ZOLL Circulation	Device Malfunction	18 states
2 Nov 2022Device	CLASS II	AutoPulse Li-ion Battery used on the AutoPulse Resuscitation System recalled	ZOLL Circulation	Device Malfunction	47 states
13 Oct 2021Device	CLASS II	Zoll, REF 8700-0782-03 (IC-3893AE), ICY Intravascular Heat recalled	ZOLL Circulation	Sterility	Nationwide
13 Oct 2021Device	CLASS II	Zoll REF: 8700-0783-01 (IC-4593) recalled by ZOLL Circulation	ZOLL Circulation	Sterility	Nationwide
13 Oct 2021Device	CLASS II	Zoll REF: 8700-0783-14 (IC-4593CO), Quattro Intravascular Heat recalled	ZOLL Circulation	Sterility	Nationwide
13 Oct 2021Device	CLASS II	Zoll REF: 8700-0783-40 (IC-4593AE), Quattro Intravascular Heat recalled	ZOLL Circulation	Sterility	Nationwide
13 Oct 2021Device	CLASS II	Zoll REF: 8700-0782-01 (IC-3893), ICY Intravascular Heat Exchange recalled	ZOLL Circulation	Sterility	Nationwide
13 Oct 2021Device	CLASS II	Zoll, REF 8700-000869-40, Cool Line (Heparin) Ivtm Disposable Pack recalled	ZOLL Circulation	Packaging Defects	Nationwide
13 Oct 2021Device	CLASS II	Zoll, REF 8700-000766-01, Quattro Ivtm Premium Disposable Pack recalled	ZOLL Circulation	Packaging Defects	Nationwide
13 Oct 2021Device	CLASS II	Zoll, REF 8700-000872-40, Solex 7(Heparin) Ivtm Disposable Pack recalled	ZOLL Circulation	Packaging Defects	Nationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.