CLASS II Device recall · Reported 13 Oct 2021 · FDA Enforcement Report
Zoll REF: 8700-0782-01 (IC-3893), ICY Intravascular Heat Exchange recalled
ZOLL Circulation is recalling Zoll REF: 8700-0782-01 (IC-3893), ICY Intravascular Heat Exchange, distributed nationwide in the US. The recall was initiated on 6 Aug 2021 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-0039-2022
- FDA event ID
- 88671
- Recalling firm
- ZOLL Circulation, San Jose, CA
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 6 Aug 2021
- FDA classified
- 6 Oct 2021
- Reported
- 13 Oct 2021
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Sterility
- Device type
- Heart & Vascular Devices
Timeline
| 6 Aug 2021 | Recall initiated by company | |
| 6 Oct 2021 | Classified by FDA | +61 days |
| 13 Oct 2021 | Published in enforcement report | +7 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Labeling update concerning potential leaks from the catheter or the start-up kit (SUK) tubing
A sterility recall means a product that must be sterile, such as an injection or eye drop, may be contaminated. Using a non-sterile product can cause serious infection.
Product as listed by the FDA
Zoll REF: 8700-0782-01 (IC-3893), ICY Intravascular Heat Exchange Catheter Kit, with central venous infusion capabilities (3 lumens) , Femoral vein Insertion Only, Sterile EO, Rx Only, UDI: (01)00849111075237
Where it was distributed
Worldwide distribution - US Nationwide distribution in the states of AL, AZ, CA, CO, FL, GA, HI, IA, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, NE, NH, NJ, NV, NY, OH, OK, OR, PA, SC, TN, TX, VA, WA, WI, WV and the countries Australia, CANADA, CHINA, GERMANY, HUNGARY, PORTUGAL, SINGAPORE, TAIWAN, THAILAND.
Nationwide AlabamaArizonaCaliforniaColoradoFloridaGeorgiaHawaiiIowaIllinoisIndianaKansasKentuckyLouisianaMassachusettsMarylandMichiganMinnesotaMissouriMississippiMontana
Questions about this recall
Is Zoll REF: 8700-0782-01 (IC-3893), ICY Intravascular Heat Exchange recalled?
Yes. ZOLL Circulation recalled Zoll REF: 8700-0782-01 (IC-3893), ICY Intravascular Heat Exchange on 6 Aug 2021. The recall is Class II and its status is Terminated. Recall number Z-0039-2022.
Why was it recalled?
Labeling update concerning potential leaks from the catheter or the start-up kit (SUK) tubing
Which lots are affected?
All Lots
Where was it sold?
Worldwide distribution - US Nationwide distribution in the states of AL, AZ, CA, CO, FL, GA, HI, IA, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, NE, NH, NJ, NV, NY, OH, OK, OR, PA, SC, TN, TX, VA, WA, WI, WV and the countries Australia, CANADA, CHINA, GERMANY, HUNGARY, PORTUGAL, SINGAPORE, TAIWAN, THAILAND.
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
More recalls from ZOLL Circulation
All 33| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS I | AutoPulse NXT Resuscitation System AutoPulse NXT Platform recalled | ZOLL Circulation | Device Malfunction | 18 states |
| Device | CLASS II | AutoPulse Li-ion Battery used on the AutoPulse Resuscitation System recalled | ZOLL Circulation | Device Malfunction | 47 states |
| Device | CLASS II | Zoll, REF 8700-0782-03 (IC-3893AE), ICY Intravascular Heat recalled | ZOLL Circulation | Sterility | Nationwide |
| Device | CLASS II | Zoll REF: 8700-0783-01 (IC-4593) recalled by ZOLL Circulation | ZOLL Circulation | Sterility | Nationwide |
| Device | CLASS II | Zoll REF: 8700-0783-14 (IC-4593CO), Quattro Intravascular Heat recalled | ZOLL Circulation | Sterility | Nationwide |
Other Heart & Vascular Devices recalls
All 6,190| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Presource Packs Containing CliniClean Pericare Wipes within recalled | Cardinal Health 200 | Other | Nationwide |
| Device | CLASS II | Presource Packs Containing CliniClean Pericare Wipes within recalled | Cardinal Health 200 | Other | Nationwide |
| Device | CLASS II | Presource Packs Containing CliniClean Pericare Wipes within recalled | Cardinal Health 200 | Other | Nationwide |
| Device | CLASS II | Presource Packs Containing CliniClean Pericare Wipes within recalled | Cardinal Health 200 | Other | Nationwide |
| Device | CLASS II | Presource Packs Containing CliniClean Pericare Wipes within recalled | Cardinal Health 200 | Other | Nationwide |