MediTrace Cadence Adult Multi-Function Defibrillation Electrodes Item Code:22550PC
Reported: September 9, 2015 Initiated: August 19, 2015 #Z-2545-2015
Product Description
MediTrace Cadence Adult Multi-Function Defibrillation Electrodes Item Code:22550PC
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 clinician burns
Details
- Recalling Firm
- Covidien LLC
- Units Affected
- 7660 sets
- Distribution
- Nationwide Foreign: Canada Australia Denmark Germany New Zealand
- Location
- North Haven, CT
Frequently Asked Questions
What product was recalled? ▼
MediTrace Cadence Adult Multi-Function Defibrillation Electrodes Item Code:22550PC. Recalled by Covidien LLC. Units affected: 7660 sets.
Why was this product recalled? ▼
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 clinician burns
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on September 9, 2015. Severity: Moderate. Recall number: Z-2545-2015.
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