Reported Oct 16, 2024 · Ongoing
iCast Covered Stent, 6MMx16MMx120CM, Model Number 42616
Atrium Medical 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: Atrium Medical Corporation · 40 Continental Blvd · Merrimack, NH · 03054-4332
Is this the product you have?
iCast Covered Stent6MMx16MMx120CMModel Number 42616
- Lot codes and dates
- UDI-DI00650862426168
- Lot Number508083
- Serial Numbers
508083031508083032508083034508083035508083036508083037508083038508083039508083040508083041508083042
- Amount recalled
- 11 devices
Where it was sold
Why it was recalled
There is an error in the Unique Device Identifier (UDI) printed on the product's distribution label.
This product could cause temporary or reversible health problems — stop using it.
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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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