Device recall
Z-2090-2014: Zoll Circulation LifeBand Single Pack (accessory), and Nickel-metal hydride…
FDA device recall · Class III · Zoll Circulation, Inc.
Key facts
| Recall number (Z-number) | Z-2090-2014 |
|---|---|
| Recall event | 68718 |
| Product | Zoll Circulation LifeBand Single Pack (accessory), and Nickel-metal hydride (NIMH) Battery. The LifeBand is a chest compression assembly that consists of a cover plate and two bands integrated with a compression pad with a Velcro fastener. The AutoPulse Battery is a removable component that supplies… |
| Product code | DRM |
| Recalling firm | Zoll Circulation, Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jul 22, 2014 |
| 510(k) numbers | K011046, K022345, K032852, K040453 |
| FEI number | 3003793491 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database