Reported Nov 11, 2020 · Terminated
Angiodynamics 5F Standard Micro-Introducer Kit - indicated for percutaneous introduction of a guidewire or catheter…
Angiodynamics, Inc.
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: Angiodynamics, Inc. · 603 Queensbury Ave · Queensbury, NY · 12804-7619
Is this the product you have?
- Angiodynamics 5F Standard Micro-Introducer Kit - indicated for percutaneous introduction of a guidewire or catheter into the vascular system
- Catalog Number06597035
- UPNH787065970355
- Lot codes and dates
- Lot Number5626935
- Expiration Date08/31/2023
- Amount recalled
- 32 kits
Where it was sold
Why it was recalled
5F Micro-Introducer Kits may not contain the correct device, packaged with a 4F Sheath/Dilator component
This product could cause temporary or reversible health problems — stop using it.
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