Device recall
Z-2625-2011: 12-lead ECG Cable Assembly contains the following cable and attachments: Main…
FDA device recall · Class III · Physio Control, Inc.
Key facts
| Recall number (Z-number) | Z-2625-2011 |
|---|---|
| Recall event | 58822 |
| Product | 12-lead ECG Cable Assembly contains the following cable and attachments: Main Cable with Limb Leads: The main cable includes the proximal connector which attaches to the monitor and four incorporated limb lead wires that terminate with ECG electrode snaps. All signals travel through this cable for… |
| Product code | MKJ |
| Recalling firm | Physio Control, Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Aug 12, 2011 |
| 510(k) numbers | K973486 |
| FEI number | 3015876 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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