Reported Nov 19, 2014 · Terminated
Medtronic Launcher Coronary Guide Catheter; MODEL: LA6JR40K
Medtronic Vascular
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: Medtronic Vascular · 35-37A Cherry Hill Drive · Danvers, MA · 01923-2565
Is this the product you have?
- Medtronic Launcher Coronary Guide Catheter
- MODELLA6JR40K
- Lot codes and dates
- Lot Number0007244836
- MODELLA6JR40K
- Amount recalled
- 11 devices
Where it was sold
Why it was recalled
Two reports have been received on the 6F launcher Guide Catheter lot (Model Number LA6JR40K; lot No 0007244836} for incorrect usable length of the Guide Catheter. It was reported that the catheters had a usable length of 90 cm instead of 55 cm, which was specified on the packaging label. Usable length is defined as the total length of catheter shaft from the distal end of the strain relief to the
This product could cause temporary or reversible health problems — stop using it.
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