ZOLL Circulation, Inc.
6 FDA 510(k) clearances · Recalling firm
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| Record | Firm | Date |
|---|---|---|
| Brand Name: AutoPulse NXT Resuscitation System Product Name: AutoPulse NXT Platform Model/ recall (Z-1533-2025) | ZOLL Circulation, Inc. | 2025-04-11 |
| AutoPulse Li-ion Battery used on the AutoPulse Resuscitation System Model 100. used as an recall (Z-0118-2023) | ZOLL Circulation, Inc. | 2022-10-21 |
| 7F NeuroFlo Catheter, Model 1027 The NeuroFlo Catheter is a multi-lumen device with two ba recall (Z-0477-2015) | ZOLL Circulation, Inc. | 2014-12-03 |
| Zoll Circulation LifeBand Single Pack (accessory), and Nickel-metal hydride (NIMH) Battery recall (Z-2090-2014) | Zoll Circulation, Inc. | 2014-07-22 |
| AutoPulse Resuscitation System Model 100, Mfg by:Zoll Circulation Sunnyvale, CA. The AutoP recall (Z-0658-2013) | Zoll Circulation, Inc. | 2013-01-09 |
| Zoll Auto Pulse Resuscitation System; Zoll Circulation Inc., Sunnyvale, CA 94085 Cardiac C recall (Z-1904-2011) | Zoll Circulation, Inc. | 2011-04-07 |
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Every clearance here is in the API, with alerts when new ones post.