Reported Nov 6, 2019 · Terminated
Cordis MAXI LD PTA Dilatation Catheter, for cardiovascular use.
Cordis Corporation
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: Cordis Corporation · 14201 NW 60th Ave · Miami Lakes, FL · 33014-2802
Is this the product you have?
- Cordis MAXI LD PTA Dilatation Catheter, for cardiovascular use.
- Lot codes and dates
- Catalog Number4171460S
- Lot Number82169860
- Expiry Date10/31/2020
- Amount recalled
- 21 units
Where it was sold
Why it was recalled
Product was manufactured utilizing an expired inner body.
This product could cause temporary or reversible health problems — stop using it.
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