Reported Nov 15, 2023 · Ongoing
Cordis ANGIOGRAPHIC CATHETERIZATION SETS, INFINITI THRULEMEN, 5F, REF CO0208, cardiac catheter
Cordis US Corp.
High riskUsing this product could cause serious injury, illness or death — stop using it now.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 US Corp · 14201 Nw 60th Ave · Miami Lakes, FL · 33014-2802
Is this the product you have?
- Cordis ANGIOGRAPHIC CATHETERIZATION SETS, INFINITI THRULEMEN, 5F, REF CO0208, cardiac catheter
- Lot codes and dates
UDI/DI 10705032025935Lot Number 18223410
- Amount recalled
- 30 devices
Where it was sold
Why it was recalled
Stop using this product now
Non-sterile product labeled as sterile was distributed.
Using this product could cause serious injury, illness or death — stop using it now.
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