Reported May 8, 2013 · Terminated
Medi-Trace Cadence Adult Radiotransparent Defibrillation Electrode Product ID: 22550R. Intended for use in…
Covidien LLC
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Covidien LLC · 15 Hampshire Street · Mansfield, MA · 02048-1113
Is this the product you have?
- Medi-Trace Cadence Adult Radiotransparent
- Defibrillation Electrode Product ID22550R. Intended for use in cardioversion, pacing, ECG monitoring, and defibrillation procedures
- Lot codes and dates
- Lot Numbers
226543X230054X230814X232182X232805X234245X304667X301844X300446X305320X
- Lot Numbers
- Amount recalled
- 133470 (sets of 2)
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
- Nationwide
Why it was recalled
Defibrillation Electrodes may arc/spark result in thermal damage to the leadwire, which could render the device incapable of delivering the appropriate energy or shock to the patient
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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