MediTrace Cadence Adult Multi-Function Defibrillation recall
MediTrace Cadence Adult Multi-Function Defibrillation Electrodes Item Code:22550PC
Why was MediTrace Cadence Adult Multi-Function Defibrillation 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
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot Numbers: 517521X, 519835X
- Product
- MediTrace Cadence Adult Multi-Function Defibrillation Electrodes Item Code:22550PC
- Recalling firm
- Covidien LLC
- Quantity
- 7660 sets
- Distribution
- Nationwide Foreign: Canada Australia Denmark Germany New Zealand
- Recall date
- September 9, 2015
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)