Drug recall
Skintact ECG Electrode FS-50, Catalog no. 58028, & Stable Base ECG Electrode SBT-60, Catalog no. 50547. To…
FDA recall event 70704 · Class II · Leonhard Lang Medizintechnik GmbH
Key facts
| Event ID | 70704 |
|---|---|
| Recall numbers | Z-1350-2015 |
| Recalling firm | Leonhard Lang Medizintechnik GmbH |
| Product type | Devices |
| Products | Skintact ECG Electrode FS-50, Catalog no. 58028 , & Stable Base ECG Electrode SBT-60, Catalog no. 50547. To acquire and transmit the electrical signal at the body surface to a processor that produces… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The electrodes may fail to transmit signals. |
| Initiation date | Feb 24, 2015 |
| Report date | Apr 8, 2015 |
| Termination date | Jul 26, 2017 |
| City | Innsbruck |
| Country | Austria |
| FEI number | 6736 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: