Drug recall
MediTrace Cadence Adult Multi-Function Defibrillation Electrodes Item Code:22550PC
FDA recall event 71963 · Class II · Covidien LLC
Key facts
| Event ID | 71963 |
|---|---|
| Recall numbers | Z-2545-2015, Z-2546-2015, Z-2547-2015 |
| Recalling firm | Covidien LLC |
| Product type | Devices |
| Products | MediTrace Cadence Adult Multi-Function Defibrillation Electrodes Item Code:22550PC, MediTrace Cadence Adult Zoll, Preconnect Defibrillation Electrode, Nonsterile Item Code:22770PC, Physio-Control Quik Combo Pacing/Defibrillation/ECG Electrodes Redi Pak¿ Preconnect System Item Code:PM20022 |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Multi-Function Defibrillation Electrodes, Pre connect- potential for damage to the wire insulation may result in a potentially increased risk for reduced or no patient therapy and patient and/or… |
| Initiation date | Aug 19, 2015 |
| Report date | Sep 9, 2015 |
| Termination date | May 24, 2017 |
| City | North Haven |
| State | CT |
| Country | United States |
| FEI number | 1219930 |
At a glance
- 1–9 Products in this recall
- 10–99 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: