Device recall
Z-2136-2011: HealthPort BioAnologics Patient Electrode Sensor Test Kit, Part # SEN-0025-0, 25…
FDA device recall · Class II · Vermed, Inc.
Key facts
| Recall number (Z-number) | Z-2136-2011 |
|---|---|
| Recall event | 58052 |
| Product | HealthPort BioAnologics Patient Electrode Sensor Test Kit, Part # SEN-0025-0, 25 kits/carton Each kit contains 100 tab electrodes and 26 alcohol pads. The electrodes are used to measure bodyfat analysis. The alcohol pads (non-sterile) are used for cleaning the skin to help the electrodes adhere… |
| Product code | IKD |
| Recalling firm | Vermed, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 25, 2011 |
| FEI number | 1317188 |
At a glance
- None 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